Canonical Allele Identifier: PA916045319
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331979
ClinVar RCV Id: RCV000295204 RCV000320092 RCV000350156 RCV000374784 RCV000870579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val951Ala
CA1944195
NM_001365536.1:c.2852T>C