Canonical Allele Identifier: PA2825131476
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519412
ClinVar RCV Id: RCV000620033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1432Trp
CA352145547
NM_000335.5:c.4294G>T