Allele Registry

Canonical Allele Identifier: PA658669190

Gene: MET HGNC NCBI

ClinVar Allele:

455993

ClinVar RCV:

RCV000532694

RCV000569043

RCV000764682

RCV001547448

RCV003470697

ClinVar Variation:

454188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ala48Thr	CA4447946 NM_001127500.3:c.142G>A CA3054204802 NM_001127500.3:c.142_144delinsACA