Canonical Allele Identifier: PA181517
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67656
ClinVar RCV Id: RCV000148863 RCV000154845 RCV000617704 RCV001144225 RCV001144226 RCV001144227 RCV001144228 RCV000987232 RCV001842275 RCV003539777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu446Lys
CA014706
NM_000335.5:c.1336G>A