Canonical Allele Identifier: PA2825038682
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1521931
ClinVar RCV Id: RCV002034165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Arg1054Gly
CA6988792
NM_000053.4:c.3160A>G