Allele Registry

Canonical Allele Identifier: PA2741994919

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV003914138

ClinVar Variation:

3037178

HGVS (amino-acid)	Matching Registered Transcripts
NP_115859.2:p.Arg548His	CA136895846 NM_032470.4:c.1643G>A