Canonical Allele Identifier: PA2825942127
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3062283
ClinVar RCV Id: RCV003986005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe1472Ile
CA352145255
NM_001160160.2:c.4414T>A