Allele Registry

Canonical Allele Identifier: PA2499253387

Gene: TNXB HGNC NCBI

ClinVar Allele:

1196003

ClinVar RCV:

RCV001572823

RCV001579579

RCV002414273

RCV003980706

ClinVar Variation:

1205924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Arg3558His	CA3733177 NM_001365276.2:c.10673G>A