Canonical Allele Identifier: PA265729
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67947
ClinVar RCV Id: RCV000058732 RCV000183093 RCV000618797 RCV002054906 RCV003996548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1660Val
CA018806
NM_001099404.2:c.4978A>G