Canonical Allele Identifier: PA2826772172
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266022
ClinVar RCV Id: RCV000256464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276947.1:p.Arg32Thr
CA10588948
NM_001290018.2:c.95G>C