Canonical Allele Identifier: PA2827326196
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 193969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile851Val
CA200886
NM_001330578.2:c.2551A>G