Allele Registry

Canonical Allele Identifier: PA2827254305

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628747

RCV001015499

RCV002477372

ClinVar Variation:

524868

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.His362Arg	CA164897661 NM_001324402.2:c.1085A>G