Canonical Allele Identifier: PA2825566050
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445551
ClinVar RCV Id: RCV003154960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106963.1:p.Phe299Leu
CA8793546
NM_001113491.2:c.897C>G
CA401208038
NM_001113491.2:c.895T>C
CA401208043
NM_001113491.2:c.897C>A