Allele Registry

Canonical Allele Identifier: PA2825622232

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003369926

ClinVar Variation:

2612857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Val1238Phe	CA368991472 NM_001127500.3:c.3712G>T