Canonical Allele Identifier: PA2826365063
Gene: AP4S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 521909
ClinVar RCV Id: RCV000622777 RCV001849416
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001241657.1:p.Leu6Pro
CA389358554
NM_001254728.2:c.17T>C