Canonical Allele Identifier: PA645428428
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309741
ClinVar RCV Id: RCV000313149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Asn22Ser
CA6599372
NM_015665.6:c.65A>G