Canonical Allele Identifier: PA2827065623
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160048
ClinVar RCV Id: RCV004452950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308443.1:p.Asn291Tyr
CA1826129
NM_001321514.2:c.871A>T