Canonical Allele Identifier: PA2825104092
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1398370
ClinVar RCV Id: RCV001893530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Arg1227Gly
CA368991551
NM_000245.4:c.3679A>G