Allele Registry

Canonical Allele Identifier: PA2825386340

Gene: TIRAP HGNC NCBI

ClinVar RCV:

RCV001703253

ClinVar Variation:

1285058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034750.1:p.Asp96Asn	CA6354644 NM_001039661.1:c.286G>A