Allele Registry

Canonical Allele Identifier: PA916045185

Gene: TNXB HGNC NCBI

ClinVar Allele:

153865

ClinVar RCV:

RCV000133610

RCV001312052

ClinVar Variation:

144113

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Thr3257Ile	CA170656 NM_001365276.2:c.9770C>T