Canonical Allele Identifier: PA645485663
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266022
ClinVar RCV Id: RCV000256464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061896.1:p.Arg32Thr
CA10588948
NM_019023.5:c.95G>C