Allele Registry

Canonical Allele Identifier: PA170655

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV002051653

ClinVar Variation:

144112

HGVS (amino-acid)	Matching Registered Transcripts
NP_115859.2:p.Arg503Cys	CA170653 NM_032470.4:c.1507C>T