Canonical Allele Identifier: PA2826836880
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682627
ClinVar RCV Id: RCV002239925 RCV004045124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280624.1:p.Arg271Leu
CA401207976
NM_001293695.2:c.812G>T