Canonical Allele Identifier: PA2825567061
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 157523
ClinVar RCV Id: RCV000144865 RCV003546477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106968.1:p.Arg38His
CA270926
NM_001113496.2:c.113G>A