Canonical Allele Identifier: PA2827326758
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Pro1063Arg
CA6988687
NM_001330578.2:c.3188C>G