Canonical Allele Identifier: PA2828305506
Gene: AP1S2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302899
ClinVar RCV Id: RCV001756398
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355936.1:p.Leu15Arg
CA412459498
NM_001369007.1:c.44T>G