Canonical Allele Identifier: PA308069
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67812
ClinVar RCV Id: RCV000058587 RCV000183184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1230Lys
CA017410
NM_000335.5:c.3688G>A