Canonical Allele Identifier: PA307627
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201505
ClinVar RCV Id: RCV000183061 RCV000617866 RCV000987203 RCV001842920 RCV003150057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1356Val
CA017845
NM_000335.5:c.4067C>T