Canonical Allele Identifier: PA211860
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67693
ClinVar RCV Id: RCV000058457 RCV000148861 RCV000413033 RCV000779409 RCV001842300 RCV002477195 RCV004019039 RCV004537259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu619Phe
CA015443
NM_000335.5:c.1855C>T