Canonical Allele Identifier: PA2827329268
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2581394
ClinVar RCV Id: RCV003331799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.His805Leu
CA388034438
NM_001330579.2:c.2414A>T