Canonical Allele Identifier: PA2829720877
Gene: TRIM29 HGNC NCBI

Linked Data

ClinVar Variation Id: 3182351
ClinVar RCV Id: RCV004473765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036233.2:p.Asp87Asn
CA6322804
NM_012101.4:c.259G>A