Allele Registry

Canonical Allele Identifier: PA2829900906

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000252128

RCV001598642

ClinVar Variation:

261117

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Asn3972Thr	CA3732914 NM_019105.8:c.11915A>C