Canonical Allele Identifier: PA2580189512
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445551
ClinVar RCV Id: RCV003154960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280625.1:p.Phe75Leu
CA8793546
NM_001293696.2:c.225C>G
CA401208038
NM_001293696.2:c.223T>C
CA401208043
NM_001293696.2:c.225C>A