Canonical Allele Identifier: PA2827921537
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68044
ClinVar RCV Id: RCV000058847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asn275Lys
CA019829
NM_001354701.2:c.825C>A
CA352150624
NM_001354701.2:c.825C>G