Canonical Allele Identifier: PA2828047193
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gly279Cys
CA007675
NM_001355216.1:c.835G>T