Canonical Allele Identifier: PA2825130948
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2850307
ClinVar RCV Id: RCV003688243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys1197Arg
CA352138139
NM_000335.5:c.3589T>C