Canonical Allele Identifier: PA2827325657
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2198694
ClinVar RCV Id: RCV002633808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Phe608Ser
CA250061564
NM_001330578.2:c.1823T>C