Allele Registry

Canonical Allele Identifier: PA2826959833

Gene: TVP23B HGNC NCBI

ClinVar Allele:

2209858

ClinVar RCV:

RCV004076319

ClinVar Variation:

2217350

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303853.1:p.Phe42Leu	CA8435086 NM_001316924.2:c.124T>C CA8435087 NM_001316924.2:c.126C>G CA398665994 NM_001316924.2:c.126C>A