Allele Registry

Canonical Allele Identifier: PA916019129

Gene: AP2S1 HGNC NCBI

ClinVar RCV:

RCV000032621

RCV000520417

ClinVar Variation:

39426

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288005.1:p.Arg31His	CA130283 NM_001301076.2:c.92G>A