Canonical Allele Identifier: PA2825129690
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 927387
ClinVar RCV Id: RCV001841115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala658Ser
CA352145050
NM_000335.5:c.1972G>T