Canonical Allele Identifier: PA2828047191
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gly279Ser
CA007667
NM_001355216.1:c.835G>A