Canonical Allele Identifier: PA2826147190
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266023
ClinVar RCV Id: RCV000256485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171753.1:p.Arg337Gly
CA8127340
NM_001184824.1:c.1009A>G