ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826772172
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_001276947.1:p.Arg32Thr
CA10588948
NM_001290018.2:c.95G>C