Canonical Allele Identifier: PA2827065405
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160048
ClinVar RCV Id: RCV004452950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308440.1:p.Asn116Tyr
CA1826129
NM_001321511.2:c.346A>T