Allele Registry

Canonical Allele Identifier: PA658803564

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628747

RCV001015499

RCV002477372

ClinVar Variation:

524868

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.His810Arg	CA164897661 NM_001127500.3:c.2429A>G