Allele Registry

Canonical Allele Identifier: PA658669356

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000567437

RCV000821666

RCV001293997

ClinVar Variation:

485767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser548Leu	CA4448215 NM_001127500.3:c.1643C>T