Canonical Allele Identifier: PA202467
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 196600
ClinVar RCV Id: RCV000177430 RCV000559336 RCV001117608 RCV001119197 RCV001706134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653197.2:p.Lys95Arg
CA202465
NM_144596.4:c.284A>G