Allele Registry

Canonical Allele Identifier: PA2825102742

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001069890

ClinVar Variation:

863031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Pro514Gln	CA368975004 NM_000245.4:c.1541C>A