Canonical Allele Identifier: PA916017081
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 437079
ClinVar RCV Id: RCV000502817 RCV000514165 RCV001085151 RCV001117716 RCV001117717 RCV003915396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275710.1:p.Gln434Arg
CA7302697
NM_001288781.1:c.1301A>G