Canonical Allele Identifier: PA2825132654
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 207974
ClinVar RCV Id: RCV000216249 RCV000247589 RCV000234809 RCV000466757 RCV000767135 RCV001842945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1897His
CA064651
NM_000335.5:c.5690G>A