Allele Registry

Canonical Allele Identifier: PA2741861868

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003763294

ClinVar Variation:

2851599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Thr611Asn	CA368978193 NM_001324401.3:c.1832C>A