Canonical Allele Identifier: PA916054999
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 646051
ClinVar RCV Id: RCV000800262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ile788Val
CA376555835
NM_020975.6:c.2362A>G