Canonical Allele Identifier: PA2827065611
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160044
ClinVar RCV Id: RCV004452946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308443.1:p.Arg263His
CA1826171
NM_001321514.2:c.788G>A