Canonical Allele Identifier: PA1139717726
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 934355
ClinVar RCV Id: RCV001202724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Leu14Phe
CA5210892
NM_012210.3:c.40C>T