Allele Registry

Canonical Allele Identifier: PA2826236398

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000005930

ClinVar Variation:

5588

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186113.1:p.Leu568Pro	CA117628 NM_001199184.3:c.1703T>C