Canonical Allele Identifier: PA107980
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67691
ClinVar RCV Id: RCV000058455 RCV000168217 RCV000148853 RCV000151792 RCV000234973 RCV000234978 RCV000622256 RCV000521151 RCV000766786 RCV001842298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly615Glu
CA015428
NM_198056.3:c.1844G>A