Canonical Allele Identifier: PA330131
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67923
ClinVar RCV Id: RCV000058704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Phe1594Ser
CA018543
NM_198056.3:c.4781T>C