Canonical Allele Identifier: PA645453732
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324515
ClinVar RCV Id: RCV000310505 RCV000341016 RCV000365211 RCV000406650 RCV000408216 RCV002524435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asn1570Ser
CA8708911
NM_000334.4:c.4709A>G