Allele Registry

Canonical Allele Identifier: PA916027459

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628755

RCV001010899

RCV001312217

ClinVar Variation:

524876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Glu6Lys	CA368972893 NM_001324402.2:c.16G>A