Canonical Allele Identifier: PA2826863051
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288010.1:p.Arg17Cys
CA130281
NM_001301081.3:c.49C>T