Canonical Allele Identifier: PA658800611
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 543804
ClinVar RCV Id: RCV000654656 RCV000764142 RCV000992893 RCV001126957 RCV001126959 RCV001126956 RCV001126958 RCV003303080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly902Ser
CA8709518
NM_000334.4:c.2704G>A