Canonical Allele Identifier: PA2829939197
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227510
ClinVar RCV Id: RCV004524628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Tyr52Ser
CA376770209
NM_020630.6:c.155A>C