Canonical Allele Identifier: PA093161
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5913
ClinVar RCV Id: RCV000006276 RCV000020262 RCV000206901 RCV001092728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg672Gly
CA253653
NM_000334.4:c.2014C>G