Canonical Allele Identifier: PA645485664
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266023
ClinVar RCV Id: RCV000256485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061896.1:p.Arg387Gly
CA8127340
NM_019023.5:c.1159A>G