Canonical Allele Identifier: PA2826862948
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39424
ClinVar RCV Id: RCV000032619 RCV001228882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288007.1:p.Arg15Cys
CA130281
NM_001301078.2:c.43C>T