Canonical Allele Identifier: PA645453487
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 255847
ClinVar RCV Id: RCV000241827 RCV000262834 RCV000287379 RCV000322477 RCV000443497 RCV000377076 RCV001082530
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Glu908Lys
CA8709512
NM_000334.4:c.2722G>A