Allele Registry

Canonical Allele Identifier: PA2828735419

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256485

ClinVar Variation:

266023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364952.1:p.Arg308Gly	CA8127340 NM_001378023.1:c.922A>G