Canonical Allele Identifier: PA2827329731
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3071932
ClinVar RCV Id: RCV004011962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr992Ala
CA388029811
NM_001330579.2:c.2974A>G