Allele Registry

Canonical Allele Identifier: PA2827596359

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256464

ClinVar Variation:

266022

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338072.1:p.Arg32Thr	CA10588948 NM_001351143.1:c.95G>C