Canonical Allele Identifier: PA2499249707
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1163359
ClinVar RCV Id: RCV001508346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile688Phe
CA388024863
NM_001330578.2:c.2062A>T