Canonical Allele Identifier: PA2828048150
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13931
ClinVar RCV Id: RCV000014956 RCV000021842 RCV000431893 RCV000432579 RCV000421871 RCV000439063 RCV000445341 RCV000426010 RCV001015022 RCV002280861 RCV001811141
ClinVar Variation Id: 38611
ClinVar RCV Id: RCV000032037 RCV000410061 RCV000411546 RCV002426530 RCV002307370
ClinVar Variation Id: 2573246
ClinVar RCV Id: RCV003316935 RCV004009734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Glu514Asp
CA008641
NM_001355216.1:c.1542G>C
CA008648
NM_001355216.1:c.1542G>T
CA2580615458
NM_001355216.1:c.1542_1545delinsCCTT