Canonical Allele Identifier: PA645447834
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Met793Ile
CA4448452
NM_001127500.3:c.2379G>T
CA368982372
NM_001127500.3:c.2379G>A
CA368982373
NM_001127500.3:c.2379G>C