Canonical Allele Identifier: PA2573193152
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1429899
ClinVar RCV Id: RCV001939162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Val721Leu
CA413598550
NM_001282224.2:c.2161G>T
CA413598551
NM_001282224.2:c.2161G>C