Allele Registry

Canonical Allele Identifier: PA2829900813

Gene: TNXB HGNC NCBI

ClinVar Allele:

1196003

ClinVar RCV:

RCV001572823

RCV001579579

RCV002414273

RCV003980706

ClinVar Variation:

1205924

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Arg3556His	CA3733177 NM_019105.8:c.10667G>A