Canonical Allele Identifier: PA915975838
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106965.1:p.Arg99Trp
CA340468
NM_001113493.2:c.295C>T