Canonical Allele Identifier: PA2825038721
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073800
ClinVar RCV Id: RCV004016806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Glu1086Asp
CA388028923
NM_000053.4:c.3258G>T
CA388028926
NM_000053.4:c.3258G>C