Allele Registry

Canonical Allele Identifier: PA658678548

Gene: TTC21B HGNC NCBI

ClinVar Allele:

440060

ClinVar RCV:

RCV000516137

ClinVar Variation:

446648

HGVS (amino-acid)	Matching Registered Transcripts
NP_079029.3:p.Ala44Asp	CA349056195 NM_024753.5:c.131C>A