Canonical Allele Identifier: PA2825279704
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1933084
ClinVar RCV Id: RCV002649576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn730Tyr
CA388034395
NM_001005918.3:c.2188A>T