Allele Registry

Canonical Allele Identifier: PA2827253185

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001069890

ClinVar Variation:

863031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Pro514Gln	CA368975004 NM_001324401.3:c.1541C>A