Canonical Allele Identifier: PA174747
Gene: INTS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161766
ClinVar RCV Id: RCV000149302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075391.3:p.Ile567Thr
CA174746
NM_023015.3:c.1700T>C