Canonical Allele Identifier: PA916012662
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 589159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Ile619Thr
CA413597501
NM_001282224.2:c.1856T>C