Canonical Allele Identifier: PA2827082039
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 314951
ClinVar RCV Id: RCV000312673 RCV003165849 RCV003930349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308780.1:p.Leu1033Phe
CA7313685
NM_001321851.1:c.3097C>T