Canonical Allele Identifier: PA645379807
Gene: PRMT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 281602
ClinVar RCV Id: RCV000376426 RCV003126662
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612373.2:p.Asp258Val
CA3098754
NM_138364.4:c.773A>T