Allele Registry

Canonical Allele Identifier: PA113850

Gene: TCN2 HGNC NCBI

ClinVar RCV:

RCV000000117

RCV000374451

RCV000454394

RCV001618205

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171655.1:p.Arg232Pro	CA113848 NM_001184726.2:c.695G>C