Canonical Allele Identifier: PA2827065547
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160048
ClinVar RCV Id: RCV004452950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308442.1:p.Asn297Tyr
CA1826129
NM_001321513.2:c.889A>T