Canonical Allele Identifier: PA2827441878
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 446138
ClinVar RCV Id: RCV000515140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335260.1:p.Arg1596Gln
CA350890921
NM_001348331.1:c.4787G>A