Allele Registry

Canonical Allele Identifier: PA215611

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000034513

RCV000535028

RCV000562476

RCV003415764

RCV003460543

ClinVar Variation:

41608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Asp340Gly	CA215608 NM_001127500.3:c.1019A>G