Canonical Allele Identifier: PA2825499399
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 288819
ClinVar RCV Id: RCV000281456 RCV001859685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.His8Gln
CA5210888
NM_001099679.2:c.24C>A
CA374647397
NM_001099679.2:c.24C>G