Canonical Allele Identifier: PA093279
Gene: SCN4A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1456Glu
CA117849
NM_000334.4:c.4367G>A