Canonical Allele Identifier: PA270928
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 157523
ClinVar RCV Id: RCV000144865 RCV003546477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006631.2:p.Arg271His
CA270926
NM_006640.5:c.812G>A