Canonical Allele Identifier: PA2825128594
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 566986
ClinVar RCV Id: RCV001771936 RCV003988852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp197Gly
CA352153531
NM_000335.5:c.590A>G