Allele Registry

Canonical Allele Identifier: PA2826870218

Gene: ACP2 HGNC NCBI

ClinVar RCV:

RCV000675645

ClinVar Variation:

558909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289419.1:p.Arg29Gln	CA5973268 NM_001302490.2:c.86G>A