Canonical Allele Identifier: PA916019128
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288005.1:p.Arg31Cys
CA130281
NM_001301076.2:c.91C>T