Canonical Allele Identifier: PA916017083
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 531831
ClinVar RCV Id: RCV000638366 RCV000765185 RCV001117719 RCV000787890 RCV001117718 RCV003928075 RCV002533215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275710.1:p.Arg459Trp
CA7302713
NM_001288781.1:c.1375C>T