Allele Registry

Canonical Allele Identifier: PA2828734962

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256485

ClinVar Variation:

266023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364949.1:p.Arg318Gly	CA8127340 NM_001378020.1:c.952A>G