Canonical Allele Identifier: PA891845968
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 586522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1587Phe
CA400615035
NM_000334.4:c.4759C>T