Canonical Allele Identifier: PA2827438182
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 801906
ClinVar RCV Id: RCV000987051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335246.1:p.Asp1615Glu
CA350892120
NM_001348317.1:c.4845T>A
CA350892123
NM_001348317.1:c.4845T>G