Allele Registry

Canonical Allele Identifier: PA916027148

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000167966

RCV000561286

RCV001293449

RCV001564694

RCV003468821

ClinVar Variation:

188112

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Leu14Phe	CA334069 NM_001324401.3:c.40C>T