Canonical Allele Identifier: PA2827325038
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1982170
ClinVar RCV Id: RCV002766624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val285Ile
CA388040902
NM_001330578.2:c.853G>A