Canonical Allele Identifier: PA916045380
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 130265
ClinVar RCV Id: RCV000176065 RCV000328939 RCV000335798 RCV000383539 RCV000422016 RCV000389147 RCV000714848 RCV001080021 RCV000768312 RCV000714847 RCV003224155 RCV002345422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asn1256Ser
CA201784
NM_001365536.1:c.3767A>G