Allele Registry

Canonical Allele Identifier: PA916027533

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000014901

RCV000079490

RCV000433739

RCV001376564

RCV002321481

RCV003407332

ClinVar Variation:

13887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.His664Arg	CA221506 NM_001324402.2:c.1991A>G