Canonical Allele Identifier: PA645428459
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 264991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Ile353Thr
CA6599005
NM_015665.6:c.1058T>C