Canonical Allele Identifier: PA891845971
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 568401
ClinVar RCV Id: RCV000688752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ile1674Val
CA8708855
NM_000334.4:c.5020A>G