Allele Registry

Canonical Allele Identifier: PA2826236294

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000005924

ClinVar Variation:

5582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186112.1:p.Ala288Thr	CA117622 NM_001199183.2:c.862G>A