Canonical Allele Identifier: PA091880
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188808
ClinVar RCV Id: RCV000169142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1101Arg
CA273987
NM_000053.4:c.3301G>A
CA388028531
NM_000053.4:c.3301G>C