Canonical Allele Identifier: PA265654
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67917
ClinVar RCV Id: RCV000058698 RCV003541165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1571Cys
CA018496
NM_001099404.2:c.4712T>G