Canonical Allele Identifier: PA329962
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67792
ClinVar RCV Id: RCV000058566 RCV000454482 RCV001842334 RCV001572250 RCV003486634 RCV004019047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1113Asn
CA017057
NM_000335.5:c.3337G>A