Allele Registry

Canonical Allele Identifier: PA2826997698

Gene: TIRAP HGNC NCBI

ClinVar RCV:

RCV000004722

RCV000004723

RCV000004724

RCV000023527

RCV001723536

RCV002490312

RCV003488326

ClinVar Variation:

4467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305706.1:p.Ser180Leu	CA116876 NM_001318777.2:c.539C>T