Canonical Allele Identifier: PA091869
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 370081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Glu1064Ala
CA6988781
NM_000053.4:c.3191A>C