Allele Registry

Canonical Allele Identifier: PA170659

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV000133611

ClinVar Variation:

144114

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Gly1331Arg	CA170658 NM_019105.8:c.3991G>A CA363431924 NM_019105.8:c.3991G>C