Canonical Allele Identifier: PA2825944857
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843
ClinVar RCV Id: RCV000058622 RCV003556153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala1276Pro
CA017704
NM_001160161.2:c.3826G>C