Canonical Allele Identifier: PA2827330011
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074411
ClinVar RCV Id: RCV004013945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala1118Val
CA6988625
NM_001330579.2:c.3353C>T