Allele Registry

Canonical Allele Identifier: PA2828173977

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000199167

RCV000998564

RCV002277552

RCV002354569

ClinVar Variation:

217018

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Asp2025Val	CA281510 NM_001365276.2:c.6074A>T