Allele Registry

Canonical Allele Identifier: PA2827253980

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628759

RCV001013433

RCV001756034

RCV002483765

ClinVar Variation:

524880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Thr191Ile	CA4448286 NM_001324402.2:c.572C>T