Canonical Allele Identifier: PA2825279238
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2146315
ClinVar RCV Id: RCV003074499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly330Glu
CA6989462
NM_001005918.3:c.989G>A