Canonical Allele Identifier: PA2827442468
Gene: TRIP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305513
ClinVar RCV Id: RCV001768720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335263.1:p.Arg350Trp
CA2153351
NM_001348334.1:c.1048C>T