Canonical Allele Identifier: PA2827064648
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160031
ClinVar RCV Id: RCV004452933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308427.1:p.Val174Leu
CA1826292
NM_001321498.2:c.520G>T
CA348067689
NM_001321498.2:c.520G>C