Canonical Allele Identifier: PA2826090177
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 309742
ClinVar RCV Id: RCV000337631 RCV000879353 RCV003930318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166937.1:p.His21Gln
CA6599373
NM_001173466.2:c.63C>G
CA385047419
NM_001173466.2:c.63C>A