Canonical Allele Identifier: PA2829939987
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477383
ClinVar RCV Id: RCV000533533 RCV000565358 RCV001103894 RCV001103892 RCV001103893 RCV001103895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Val240Leu
CA044589
NM_020630.6:c.718G>C
CA376544709
NM_020630.6:c.718G>T