Allele Registry

Canonical Allele Identifier: PA2829475643

Gene: TNFRSF10B HGNC NCBI

ClinVar RCV:

RCV003972305

ClinVar Variation:

3056241

HGVS (amino-acid)	Matching Registered Transcripts
NP_003833.4:p.Ala67Val	CA4673455 NM_003842.5:c.200C>T