Canonical Allele Identifier: PA2580134350
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_001120972.1:p.Trp972Arg
CA368986712
NM_001127500.3:c.2914T>A
CA368986714
NM_001127500.3:c.2914T>C