Canonical Allele Identifier: PA916045492
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 234820
ClinVar RCV Id: RCV000222397 RCV000359398 RCV000271832 RCV000270670 RCV000390843 RCV000514151 RCV001080948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1904His
CA1943628
NM_001365536.1:c.5711G>A