Canonical Allele Identifier: PA211875
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68032
ClinVar RCV Id: RCV000058835 RCV000148865 RCV000182942 RCV000521042 RCV000620248 RCV001842405 RCV002477205 RCV004545872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg225Trp
CA019714
NM_000335.5:c.673C>T