Canonical Allele Identifier: PA2826318073
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075602
ClinVar RCV Id: RCV004017120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly887Val
CA388032104
NM_001243182.2:c.2660G>T