Canonical Allele Identifier: PA2741850742
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2926677
ClinVar RCV Id: RCV003788915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Asn602Lys
CA413597248
NM_001282224.2:c.1806C>A
CA413597250
NM_001282224.2:c.1806C>G