Canonical Allele Identifier: PA645501180
Gene: TRIP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 314943
ClinVar RCV Id: RCV000508397 RCV003278760 RCV000893258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004230.2:p.Glu1387Lys
CA7313512
NM_004239.4:c.4159G>A