Canonical Allele Identifier: PA915955100
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 558238
ClinVar RCV Id: RCV000674475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly979Arg
CA388025845
NM_001005918.3:c.2935G>C