Allele Registry

Canonical Allele Identifier: PA2828175787

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV002051653

ClinVar Variation:

144112

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Arg4074Cys	CA170653 NM_001365276.2:c.12220C>T