Canonical Allele Identifier: PA2825103647
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1510656
ClinVar RCV Id: RCV002014028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Asp981His
CA368987130
NM_000245.4:c.2941G>C