Canonical Allele Identifier: PA658668860
Gene: SCN4A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ser804Cys
CA400627209
NM_000334.4:c.2411C>G