Allele Registry

Canonical Allele Identifier: PA916027532

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000435140

ClinVar Variation:

376068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.His664Tyr	CA16602530 NM_001324402.2:c.1990C>T