Canonical Allele Identifier: PA2499231263
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1039768
ClinVar RCV Id: RCV001343311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg1132Gly
CA400619461
NM_000334.4:c.3394C>G