Canonical Allele Identifier: PA658826460
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 557001
ClinVar RCV Id: RCV000673083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly891Asp
CA388034407
NM_000053.4:c.2672G>A