Canonical Allele Identifier: PA2829942130
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 232162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser829Gly
CA039406
NM_020630.6:c.2485A>G