Canonical Allele Identifier: PA645447826
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ser766Gly
CA4448445
NM_001127500.3:c.2296A>G