Canonical Allele Identifier: PA645428483
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Gly533Arg
CA6598796
NM_015665.6:c.1597G>A
CA385034680
NM_015665.6:c.1597G>C