Allele Registry

Canonical Allele Identifier: PA2573200650

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002004727

RCV002407169

ClinVar Variation:

1449962

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Phe596Tyr	CA368977911 NM_001324401.3:c.1787T>A