Canonical Allele Identifier: PA2499253413
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1033963
ClinVar RCV Id: RCV001336521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile740Thr
CA349079693
NM_001365536.1:c.2219T>C