Allele Registry

Canonical Allele Identifier: PA093718

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014901

RCV000079490

RCV000433739

RCV001376564

RCV002321481

RCV003407332

ClinVar Variation:

13887

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.His1094Arg	CA221506 NM_000245.4:c.3281A>G