Canonical Allele Identifier: PA916045404
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 808874
ClinVar RCV Id: RCV001041147 RCV000997294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys1386Gln
CA1943940
NM_001365536.1:c.4156A>C