Canonical Allele Identifier: PA2829977824
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067586.1:p.Arg15Cys
CA130281
NM_021575.5:c.43C>T