Allele Registry

Canonical Allele Identifier: PA337370

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000197671

RCV001025145

RCV001450055

RCV001706186

RCV003320598

ClinVar Variation:

216513

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Leu211Trp	CA337368 NM_001127500.3:c.632T>G