Allele Registry

Canonical Allele Identifier: PA915988592

Gene: TRIM31 HGNC NCBI

ClinVar RCV:

RCV000956375

ClinVar Variation:

776120

HGVS (amino-acid)	Matching Registered Transcripts
NP_008959.3:p.Arg72Trp	CA3694869 NM_007028.5:c.214C>T