Allele Registry

Canonical Allele Identifier: PA2829900948

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV003914138

ClinVar Variation:

3037178

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Arg4117His	CA136895846 NM_019105.8:c.12350G>A