Canonical Allele Identifier: PA2825103269
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1790957
ClinVar RCV Id: RCV002450372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Val788Glu
CA368982597
NM_000245.4:c.2363T>A