Allele Registry

Canonical Allele Identifier: PA645447723

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000458343

RCV000765914

RCV002393162

RCV003463962

ClinVar Variation:

411909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ala48Gly	CA4447947 NM_001127500.3:c.143C>G