Canonical Allele Identifier: PA2827065299
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160044
ClinVar RCV Id: RCV004452946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308438.1:p.Arg236His
CA1826171
NM_001321509.2:c.707G>A