Canonical Allele Identifier: PA2825566542
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 889089
ClinVar RCV Id: RCV001122816 RCV002240654 RCV004032241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106965.1:p.Val296Met
CA8793548
NM_001113493.2:c.886G>A