Canonical Allele Identifier: PA2825038820
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2794286
ClinVar RCV Id: RCV003609543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1178Pro
CA388026029
NM_000053.4:c.3532A>C