Canonical Allele Identifier: PA2826317895
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075609
ClinVar RCV Id: RCV004017127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile762Val
CA388034791
NM_001243182.2:c.2284A>G