Canonical Allele Identifier: PA2827327081
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3849
ClinVar RCV Id: RCV000004053 RCV001507825
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly1188Arg
CA252890
NM_001330578.2:c.3562G>A
CA388022028
NM_001330578.2:c.3562G>C