Canonical Allele Identifier: PA2827921681
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67633
ClinVar RCV Id: RCV000058389 RCV000182957 RCV000466350 RCV000763108 RCV002444519 RCV003987345 RCV004545743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg367Cys
CA014305
NM_001354701.2:c.1099C>T
CA645519439
NM_001354701.2:c.1098_1099delinsTT