Canonical Allele Identifier: PA916017084
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235131
ClinVar RCV Id: RCV000223936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275710.1:p.Gln465His
CA10581229
NM_001288781.1:c.1395G>C
CA390553557
NM_001288781.1:c.1395G>T