Canonical Allele Identifier: PA916058618
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450031
ClinVar RCV Id: RCV000523584
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067586.1:p.Leu63Pro
CA406507996
NM_021575.5:c.188T>C