Canonical Allele Identifier: PA916029894
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_001335259.1:p.Arg1671Gln
CA350890921
NM_001348330.2:c.5012G>A