Canonical Allele Identifier: PA916045299
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 440256
ClinVar RCV Id: RCV000507760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile856Val
CA349078055
NM_001365536.1:c.2566A>G