Canonical Allele Identifier: PA2825038039
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1467615
ClinVar RCV Id: RCV001966467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Glu385Gln
CA388038688
NM_000053.4:c.1153G>C