Allele Registry

Canonical Allele Identifier: PA2825622230

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001553682

ClinVar Variation:

1192249

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Val1238Leu	CA368991469 NM_001127500.3:c.3712G>C