Allele Registry

Canonical Allele Identifier: PA257008

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014900

ClinVar Variation:

13886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Leu1213Val	CA257006 NM_001127500.3:c.3637C>G