Canonical Allele Identifier: PA916012634
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 210393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Ile506Val
CA206236
NM_001282224.2:c.1516A>G