Canonical Allele Identifier: PA2827329230
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3065415
ClinVar RCV Id: RCV003990492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala790Gly
CA388034775
NM_001330579.2:c.2369C>G