Canonical Allele Identifier: PA2825130950
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1299874
ClinVar RCV Id: RCV001730302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1200Phe
CA352138115
NM_000335.5:c.3598A>T