Canonical Allele Identifier: PA658668939
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 448280
ClinVar RCV Id: RCV000532008 RCV002305499 RCV002267617 RCV002473036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg1451His
CA292957365
NM_000334.4:c.4352G>A