Canonical Allele Identifier: PA2825130049
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 451632
ClinVar RCV Id: RCV000519232 RCV002431487 RCV004003628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val836Met
CA060533
NM_000335.5:c.2506G>A