Canonical Allele Identifier: PA2827924122
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2119739
ClinVar RCV Id: RCV003658688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ser1946Arg
CA352139537
NM_001354701.2:c.5838C>G
CA352139539
NM_001354701.2:c.5838C>A
CA352139548
NM_001354701.2:c.5836A>C