Canonical Allele Identifier: PA2826638230
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11795
ClinVar RCV Id: RCV000012562 RCV000789728 RCV001206423 RCV001696176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Pro1308Ser
CA256077
NM_001282224.2:c.3922C>T