Allele Registry

Canonical Allele Identifier: PA2826143207

Gene: TCN2 HGNC NCBI

ClinVar RCV:

RCV001898181

ClinVar Variation:

1393171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171655.1:p.Arg232His	CA10184846 NM_001184726.2:c.695G>A