Allele Registry

Canonical Allele Identifier: PA2828735139

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256434

RCV001266541

RCV001855017

ClinVar Variation:

266021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364950.1:p.Trp415Arg	CA8127489 NM_001378021.1:c.1243T>C CA396439682 NM_001378021.1:c.1243T>A