Canonical Allele Identifier: PA2825566398
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3002773
ClinVar RCV Id: RCV003860364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106965.1:p.Ala81Val
CA8793156
NM_001113493.2:c.242C>T