Canonical Allele Identifier: PA2825566384
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682580
ClinVar RCV Id: RCV002237552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106965.1:p.Ser67Pro
CA401205737
NM_001113493.2:c.199T>C