Canonical Allele Identifier: PA307609
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67847
ClinVar RCV Id: RCV000058626 RCV000183057 RCV000456774 RCV004017378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1333Val
CA017738
NM_000335.5:c.3997A>G