Allele Registry

Canonical Allele Identifier: PA2828175743

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000252128

RCV001598642

ClinVar Variation:

261117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Asn3974Thr	CA3732914 NM_001365276.2:c.11921A>C