Canonical Allele Identifier: PA2573211219
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1412334
ClinVar RCV Id: RCV001923198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu1342Ser
CA349064198
NM_001365536.1:c.4025T>C