Canonical Allele Identifier: PA916029893
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 801906
ClinVar RCV Id: RCV000987051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335259.1:p.Asp1663Glu
CA350892120
NM_001348330.2:c.4989T>A
CA350892123
NM_001348330.2:c.4989T>G