Allele Registry

Canonical Allele Identifier: PA2827596442

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256485

ClinVar Variation:

266023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338072.1:p.Arg387Gly	CA8127340 NM_001351143.1:c.1159A>G