Canonical Allele Identifier: PA2825130792
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1038492
ClinVar RCV Id: RCV003770914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp1133Glu
CA352138553
NM_000335.5:c.3399C>G
CA352138554
NM_000335.5:c.3399C>A