Canonical Allele Identifier: PA916045352
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331972
ClinVar RCV Id: RCV000329282 RCV000335564 RCV000293562 RCV000647806 RCV000388955 RCV002450896 RCV002472991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ser1115Gly
CA1944092
NM_001365536.1:c.3343A>G