Canonical Allele Identifier: PA916045244
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6367
ClinVar RCV Id: RCV000006739 RCV000153918 RCV000415152 RCV000488281 RCV001083774 RCV001133028 RCV001133029 RCV001133030 RCV002415403 RCV004532301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys666Arg
CA118167
NM_001365536.1:c.1997A>G