Allele Registry

Canonical Allele Identifier: PA117623

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000005924

ClinVar Variation:

5582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001486.1:p.Ala304Thr	CA117622 NM_001001486.2:c.910G>A