Canonical Allele Identifier: PA099519
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 7350
ClinVar RCV Id: RCV000007775 RCV000414917 RCV000538874 RCV001198489 RCV001781203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Asp487Asn
CA118728
NM_001099679.2:c.1459G>A