Canonical Allele Identifier: PA2825566361
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682575
ClinVar RCV Id: RCV002237547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106965.1:p.Pro36Arg
CA401205548
NM_001113493.2:c.107C>G