Canonical Allele Identifier: PA916012660
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 589116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Ile612Ser
CA413597399
NM_001282224.2:c.1835T>G