Canonical Allele Identifier: PA2580108797
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1910623
ClinVar RCV Id: RCV002593400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ile1391Val
CA292958196
NM_000334.4:c.4171A>G