Canonical Allele Identifier: PA181476
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67988
ClinVar RCV Id: RCV000058775 RCV000148840 RCV000154835 RCV000474591 RCV000621224 RCV000987199 RCV001144221 RCV001144218 RCV001144219 RCV001144220 RCV001842385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1786Asn
CA019158
NM_000335.5:c.5357G>A