Canonical Allele Identifier: PA2827325640
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1979422
ClinVar RCV Id: RCV002766293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Tyr594Cys
CA250061586
NM_001330578.2:c.1781A>G