Canonical Allele Identifier: PA2829645369
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682581
ClinVar RCV Id: RCV002239911 RCV004045120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006631.2:p.Ser56Leu
CA8793142
NM_006640.5:c.167C>T