Canonical Allele Identifier: PA203843
Gene: AAAS HGNC NCBI

Linked Data

ClinVar Variation Id: 202169
ClinVar RCV Id: RCV000184015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056480.1:p.Val313Ala
CA203842
NM_015665.6:c.938T>C