Canonical Allele Identifier: PA118730
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 7350
ClinVar RCV Id: RCV000007775 RCV000414917 RCV000538874 RCV001198489 RCV001781203
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Asp487Asn
CA118728
NM_012210.3:c.1459G>A