Canonical Allele Identifier: PA645501162
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_004230.2:p.Asn1202His
CA7313606
NM_004239.4:c.3604A>C