Canonical Allele Identifier: PA2827254624
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_001311331.1:p.Trp524Arg
CA368986712
NM_001324402.2:c.1570T>A
CA368986714
NM_001324402.2:c.1570T>C