Canonical Allele Identifier: PA211838
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67682
ClinVar RCV Id: RCV000058446 RCV000148854 RCV000456073 RCV000987224 RCV003486629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala572Ser
CA015256
NM_000335.5:c.1714G>T