Canonical Allele Identifier: PA2825941362
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9388
ClinVar RCV Id: RCV000009986 RCV000058542 RCV000183020 RCV002504775 RCV004532320 RCV003591626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala997Ser
CA016718
NM_001160160.2:c.2989G>T