Allele Registry

Canonical Allele Identifier: PA645501020

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000252128

RCV001598642

ClinVar Variation:

261117

HGVS (amino-acid)	Matching Registered Transcripts
NP_115859.2:p.Asn403Thr	CA3732914 NM_032470.4:c.1208A>C