Canonical Allele Identifier: PA916045336
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 415031
ClinVar RCV Id: RCV000476670 RCV001131848 RCV001131849 RCV001131847 RCV002323791 RCV003332181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys1056Arg
CA1944130
NM_001365536.1:c.3167A>G