Canonical Allele Identifier: PA645391655
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 262515
ClinVar RCV Id: RCV000470558 RCV000253058 RCV001117604 RCV001117605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653197.2:p.Asp65Gly
CA7302389
NM_144596.4:c.194A>G