Allele Registry

Canonical Allele Identifier: PA2826745014

Gene: TTC8 HGNC NCBI

ClinVar Allele:

339735

ClinVar RCV:

RCV000304181

RCV000360976

RCV001859883

RCV003888731

ClinVar Variation:

314797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001275710.1:p.Ser2Asn	CA7302304 NM_001288781.1:c.5G>A