Canonical Allele Identifier: PA916045312
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 576791
ClinVar RCV Id: RCV000699374 RCV003437401
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Glu927Lys
CA1944205
NM_001365536.1:c.2779G>A