Canonical Allele Identifier: PA2825131478
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2875975
ClinVar RCV Id: RCV003707531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1432Arg
CA72943607
NM_000335.5:c.4294G>A
CA352145548
NM_000335.5:c.4294G>C