Canonical Allele Identifier: PA2826997698
Gene: TIRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 4467
ClinVar RCV Id: RCV000004722 RCV000004723 RCV000004724 RCV000023527 RCV001723536 RCV002490312 RCV003488326
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Amino-acid Alleles

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