Canonical Allele Identifier: PA2827922546
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2959874
ClinVar RCV Id: RCV003812049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asn958Lys
CA72926407
NM_001354701.2:c.2874C>A
CA352140418
NM_001354701.2:c.2874C>G