Canonical Allele Identifier: PA2827921176
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1035042
ClinVar RCV Id: RCV003541353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ser11Arg
CA72951853
NM_001354701.2:c.33C>A
CA352159498
NM_001354701.2:c.33C>G
CA352159521
NM_001354701.2:c.31A>C