Canonical Allele Identifier: PA307355
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201468
ClinVar RCV Id: RCV000182994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys683Arg
CA015776
NM_000335.5:c.2047T>C