Allele Registry

Canonical Allele Identifier: PA645506493

Gene: TTC21B HGNC NCBI

ClinVar RCV:

RCV000252032

RCV000861670

RCV001697725

RCV002278217

RCV002518656

ClinVar Variation:

261780

HGVS (amino-acid)	Matching Registered Transcripts
NP_079029.3:p.Val1139Ala	CA1941516 NM_024753.5:c.3416T>C