Canonical Allele Identifier: PA330047
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67878
ClinVar RCV Id: RCV000058658 RCV000414661 RCV001842360
ClinVar Variation Id: 659965
ClinVar RCV Id: RCV003539334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1431Ser
CA018093
NM_000335.5:c.4293G>C
CA352145549
NM_000335.5:c.4293G>T