Canonical Allele Identifier: PA2828735270
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266023
ClinVar RCV Id: RCV000256485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364951.1:p.Arg308Gly
CA8127340
NM_001378022.1:c.922A>G