Allele Registry

Canonical Allele Identifier: PA2825101748

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000458343

RCV000765914

RCV002393162

RCV003463962

ClinVar Variation:

411909

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Ala48Gly	CA4447947 NM_000245.4:c.143C>G