Allele Registry

Canonical Allele Identifier: PA2827253973

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000235673

RCV000573538

RCV003225052

ClinVar Variation:

246627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Thr188Met	CA4448284 NM_001324402.2:c.563C>T