Allele Registry

Canonical Allele Identifier: PA2828212632

Gene: TTC8 HGNC NCBI

ClinVar RCV:

RCV000638366

RCV000765185

RCV000787890

RCV001117718

RCV001117719

RCV002533215

RCV003928075

ClinVar Variation:

531831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001353464.1:p.Arg433Trp	CA7302713 NM_001366535.2:c.1297C>T