Canonical Allele Identifier: PA307242
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67648
ClinVar RCV Id: RCV000058405 RCV000182963 RCV004545744
ClinVar Variation Id: 67649
ClinVar RCV Id: RCV000058406 RCV001256848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asn406Lys
CA014532
NM_000335.5:c.1218C>A
CA014540
NM_000335.5:c.1218C>G