Canonical Allele Identifier: PA2827330273
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 92389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val1213Ile
CA145689
NM_001330579.2:c.3637G>A