Allele Registry

Canonical Allele Identifier: PA281511

Gene: TNXB HGNC NCBI

ClinVar Allele:

213571

ClinVar RCV:

RCV000199167

RCV000998564

RCV002277552

RCV002354569

ClinVar Variation:

217018

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Asp2025Val	CA281510 NM_019105.8:c.6074A>T