Canonical Allele Identifier: PA2573179151
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_001106963.1:p.Ser74Pro
CA401205737
NM_001113491.2:c.220T>C