Allele Registry

Canonical Allele Identifier: PA2580396151

Gene: TRIM58 HGNC NCBI

ClinVar Allele:

2220750

ClinVar RCV:

RCV004097918

ClinVar Variation:

2233897

HGVS (amino-acid)	Matching Registered Transcripts
NP_056246.3:p.Ala206Val	CA1498211 NM_015431.4:c.617C>T