Canonical Allele Identifier: PA2828734817
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266023
ClinVar RCV Id: RCV000256485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364947.1:p.Arg387Gly
CA8127340
NM_001378018.1:c.1159A>G