Canonical Allele Identifier: PA2827082105
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 290765
ClinVar RCV Id: RCV000359112 RCV000755412 RCV002278324 RCV001705435 RCV003910042 RCV002518149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Asn1201His
CA7313606
NM_001321851.1:c.3601A>C