Canonical Allele Identifier: PA916045353
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 194737
ClinVar RCV Id: RCV000655985 RCV002453614 RCV000175172 RCV001198858 RCV000540284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val1117Leu
CA240877
NM_001365536.1:c.3349G>T
CA349072403
NM_001365536.1:c.3349G>C