Canonical Allele Identifier: PA2825103597
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2495619
ClinVar Variation Id: 3232956
ClinVar RCV Id: RCV004523588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Trp954Arg
CA368986712
NM_000245.4:c.2860T>A
CA368986714
NM_000245.4:c.2860T>C