Canonical Allele Identifier: PA2825279696
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2581394
ClinVar RCV Id: RCV003331799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.His727Leu
CA388034438
NM_001005918.3:c.2180A>T