Canonical Allele Identifier: PA2827064947
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160044
ClinVar RCV Id: RCV004452946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308431.1:p.Arg255His
CA1826171
NM_001321502.2:c.764G>A