Canonical Allele Identifier: PA2829939200
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1775033
ClinVar RCV Id: RCV002403357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Tyr52His
CA376770207
NM_020630.6:c.154T>C