Canonical Allele Identifier: PA091981
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3861
ClinVar RCV Id: RCV000004065
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr766Arg
CA252898
NM_000053.4:c.2297C>G