Canonical Allele Identifier: PA2826365019
Gene: AP4S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 521909
ClinVar RCV Id: RCV000622777 RCV001849416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001241656.1:p.Leu6Pro
CA389358554
NM_001254727.2:c.17T>C