Canonical Allele Identifier: PA193974
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 186141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Val1110Ile
CA193972
NM_001127500.3:c.3328G>A