Canonical Allele Identifier: PA128873
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 30045
ClinVar RCV Id: RCV000022947 RCV000148858 RCV000154830 RCV000756620 RCV000688881 RCV001841252 RCV004018664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asn1986Lys
CA019555
NM_000335.5:c.5958C>A
CA352139301
NM_000335.5:c.5958C>G