Canonical Allele Identifier: PA2828180374
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 415032
ClinVar RCV Id: RCV000463481 RCV000768079 RCV001755714 RCV003224294 RCV002446880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met426Lys
CA1944559
NM_001365536.1:c.1277T>A