Allele Registry

Canonical Allele Identifier: PA2826997692

Gene: TIRAP HGNC NCBI

ClinVar RCV:

RCV001703253

ClinVar Variation:

1285058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305706.1:p.Asp96Asn	CA6354644 NM_001318777.2:c.286G>A