Canonical Allele Identifier: PA916045350
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 423474
ClinVar RCV Id: RCV000726838 RCV001083029 RCV002455939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ser1110Leu
CA1944100
NM_001365536.1:c.3329C>T