Allele Registry

Canonical Allele Identifier: PA2828175796

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV003914138

ClinVar Variation:

3037178

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Arg4119His	CA136895846 NM_001365276.2:c.12356G>A