Canonical Allele Identifier: PA2573193148
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1401372
ClinVar RCV Id: RCV001911777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Phe717Leu
CA413598523
NM_001282224.2:c.2149T>C
CA413598528
NM_001282224.2:c.2151T>A
CA413598529
NM_001282224.2:c.2151T>G