Canonical Allele Identifier: PA2826891833
Gene: PRMT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 281602
ClinVar RCV Id: RCV000376426 RCV003126662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291387.1:p.Asp145Val
CA3098754
NM_001304458.2:c.434A>T