Canonical Allele Identifier: PA645453427
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324539
ClinVar RCV Id: RCV000291355 RCV000325619 RCV000329956 RCV000384873 RCV000386753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asp532Asn
CA8709798
NM_000334.4:c.1594G>A