Allele Registry

Canonical Allele Identifier: PA2825103282

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628747

RCV001015499

RCV002477372

ClinVar Variation:

524868

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.His792Arg	CA164897661 NM_000245.4:c.2375A>G