Canonical Allele Identifier: PA2580134086
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1790456
ClinVar RCV Id: RCV002457909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Val794Gly
CA368982386
NM_001127500.3:c.2381T>G