Canonical Allele Identifier: PA2499253450
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1014917
ClinVar RCV Id: RCV001313719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asp1355Asn
CA349063849
NM_001365536.1:c.4063G>A