Canonical Allele Identifier: PA916045398
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 195676
ClinVar RCV Id: RCV000176293 RCV000647757 RCV002321697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1358Gln
CA242197
NM_001365536.1:c.4073G>A