Canonical Allele Identifier: PA915960983
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 705678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ala1731Thr
CA8708820
NM_000334.4:c.5191G>A