Canonical Allele Identifier: PA2825942683
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1215136
ClinVar RCV Id: RCV001583962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe1822Ser
CA352140834
NM_001160160.2:c.5465T>C