Allele Registry

Canonical Allele Identifier: PA093755

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014900

ClinVar Variation:

13886

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Leu1195Val	CA257006 NM_000245.4:c.3583C>G