Canonical Allele Identifier: PA143111
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48308
ClinVar RCV Id: RCV000041628 RCV000058787 RCV000245837 RCV000622807 RCV001507623 RCV001841611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln1831Glu
CA019294
NM_000335.5:c.5491C>G