Canonical Allele Identifier: PA2826318352
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1308069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile1083Val
CA6988631
NM_001243182.2:c.3247A>G