Canonical Allele Identifier: PA2825566207
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445551
ClinVar RCV Id: RCV003154960
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106964.1:p.Phe135Leu
CA8793546
NM_001113492.2:c.405C>G
CA401208038
NM_001113492.2:c.403T>C
CA401208043
NM_001113492.2:c.405C>A