Canonical Allele Identifier: PA093309
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5924
ClinVar RCV Id: RCV000006287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Ile141Val
CA117856
NM_000334.4:c.421A>G