Allele Registry

Canonical Allele Identifier: PA170657

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000133610

RCV001312052

ClinVar Variation:

144113

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Thr3255Ile	CA170656 NM_019105.8:c.9764C>T