Allele Registry

Canonical Allele Identifier: PA106937

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

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Glu768Asp	CA008641 NM_020975.6:c.2304G>C CA008648 NM_020975.6:c.2304G>T CA2580615458 NM_020975.6:c.2304_2307delinsCCTT