Allele Registry

Canonical Allele Identifier: PA2825102936

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003763294

ClinVar Variation:

2851599

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr611Asn	CA368978193 NM_000245.4:c.1832C>A