Canonical Allele Identifier: PA2827442494
Gene: TRIP12 HGNC NCBI
ClinVar RCV:
RCV003142831
ClinVar Variation:
2437328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335264.1:p.Asn110Ser
CA2153524
NM_001348335.2:c.329A>G