Canonical Allele Identifier: PA265331
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67822
ClinVar RCV Id: RCV000058597
ClinVar Variation Id: 2691028
ClinVar RCV Id: RCV003487111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1248Asp
CA017484
NM_000335.5:c.3743T>A
CA2697550807
NM_000335.5:c.3743_3744delinsAT