Canonical Allele Identifier: PA1139744499
Gene: PRMT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 266022
ClinVar RCV Id: RCV000256464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364949.1:p.Glu12Gln
CA10588948
NM_001378020.1:c.34G>C