Canonical Allele Identifier: PA2827329227
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala790Val
CA252892
NM_001330579.2:c.2369C>T