Canonical Allele Identifier: PA2827326322
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1708015
ClinVar RCV Id: RCV002287176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ser908Cys
CA388032277
NM_001330578.2:c.2723C>G