Canonical Allele Identifier: PA329963
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_001092874.1:p.Asp1114Asn
CA017057
NM_001099404.2:c.3340G>A