Canonical Allele Identifier: PA916012612
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 388685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Ala334Thr
CA10458981
NM_001282224.2:c.1000G>A