Canonical Allele Identifier: PA128277
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Cys634Gly
CA008324
NM_020630.6:c.1900T>G