Canonical Allele Identifier: PA915988413
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 797998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Ser357Phe
CA6599000
NM_015665.6:c.1070C>T