Canonical Allele Identifier: PA645428438
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309737
ClinVar RCV Id: RCV000393948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Val87Leu
CA6599283
NM_015665.6:c.259G>T
CA385044579
NM_015665.6:c.259G>C