Canonical Allele Identifier: PA091839
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Arg919Trp
CA6988915
NM_000053.4:c.2755C>T