Allele Registry

Canonical Allele Identifier: PA170654

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV002051653

ClinVar Variation:

144112

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Arg4072Cys	CA170653 NM_019105.8:c.12214C>T