Canonical Allele Identifier: PA2825942479
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67965
ClinVar RCV Id: RCV000058751 RCV000762372 RCV000824908 RCV001842380 RCV004019060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1706Trp
CA018994
NM_001160160.2:c.5116C>T