Canonical Allele Identifier: PA2827326086
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2581394
ClinVar RCV Id: RCV003331799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.His811Leu
CA388034438
NM_001330578.2:c.2432A>T