Canonical Allele Identifier: PA2827438990
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_001335249.1:p.Asp1657Glu
CA350892120
NM_001348320.2:c.4971T>A
CA350892123
NM_001348320.2:c.4971T>G