Allele Registry

Canonical Allele Identifier: PA2826236071

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000005924

ClinVar Variation:

5582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186109.1:p.Ala338Thr	CA117622 NM_001199180.2:c.1012G>A