Canonical Allele Identifier: PA2826090232
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309737
ClinVar RCV Id: RCV000393948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166937.1:p.Val87Leu
CA6599283
NM_001173466.2:c.259G>T
CA385044579
NM_001173466.2:c.259G>C