Canonical Allele Identifier: PA2827081868
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 5511
ClinVar RCV Id: RCV000005846 RCV000725982 RCV002276533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Asn700Ser
CA117563
NM_001321851.1:c.2099A>G