Canonical Allele Identifier: PA2826235992
Gene: ATP2C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 343324
ClinVar RCV Id: RCV000381408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186108.1:p.Ser261Asn
CA2614925
NM_001199179.3:c.782G>A