Allele Registry

Canonical Allele Identifier: PA2827596632

Gene: PRMT7 HGNC NCBI

ClinVar RCV:

RCV000256434

RCV001266541

RCV001855017

ClinVar Variation:

266021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338073.1:p.Trp494Arg	CA8127489 NM_001351144.1:c.1480T>C CA396439682 NM_001351144.1:c.1480T>A