Canonical Allele Identifier: PA2828805089
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007266
ClinVar RCV Id: RCV001304417
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Glu25Asp
CA374647507
NM_001379048.1:c.75G>T
CA374647508
NM_001379048.1:c.75G>C