Canonical Allele Identifier: PA2825566203
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_001106964.1:p.Arg126Leu
CA401207976
NM_001113492.2:c.377G>T