Canonical Allele Identifier: PA113494
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_004060.2:p.Arg15Cys
CA130281
NM_004069.6:c.43C>T