Canonical Allele Identifier: PA2828180375
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 953237
ClinVar RCV Id: RCV001225496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met426Thr
CA349085721
NM_001365536.1:c.1277T>C