Canonical Allele Identifier: PA645428425
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.His21Gln
CA6599373
NM_015665.6:c.63C>G
CA385047419
NM_015665.6:c.63C>A