Allele Registry

Canonical Allele Identifier: PA645450844

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000246888

RCV001838593

RCV001838594

RCV002278191

RCV002450782

ClinVar Variation:

261136

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.His1161Arg	CA3735168 NM_019105.8:c.3482A>G