Canonical Allele Identifier: PA916045512
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471159
ClinVar RCV Id: RCV000526962 RCV002358559 RCV003139848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ser1986Gly
CA1943590
NM_001365536.1:c.5956A>G