Canonical Allele Identifier: PA2827064785
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_001308429.1:p.Arg255His
CA1826171
NM_001321500.2:c.764G>A