Canonical Allele Identifier: PA1139675050
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 861357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Ala986Ser
CA368987204
NM_000245.4:c.2956G>T