Canonical Allele Identifier: PA2825566898
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_001106967.2:p.Phe48Leu
CA8793546
NM_001113495.2:c.144C>G
CA401208038
NM_001113495.2:c.142T>C
CA401208043
NM_001113495.2:c.144C>A