Canonical Allele Identifier: PA658818888
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_009008.2:p.Leu6Pro
CA389358554
NM_007077.5:c.17T>C