Canonical Allele Identifier: PA2829645376
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682584
ClinVar RCV Id: RCV002239914 RCV003164340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006631.2:p.Arg58Cys
CA8793147
NM_006640.5:c.172C>T