Canonical Allele Identifier: PA2826999500
Gene: TTC9C HGNC NCBI

Linked Data

ClinVar Variation Id: 2519974
ClinVar RCV Id: RCV004294913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305742.1:p.Ala117Ser
CA6054644
NM_001318813.2:c.349G>T