Canonical Allele Identifier: PA2826837385
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445473
ClinVar RCV Id: RCV003154882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280627.1:p.Arg39Gln
CA8793543
NM_001293698.2:c.116G>A