Canonical Allele Identifier: PA2825131856
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1483535
ClinVar RCV Id: RCV003657588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1596Leu
CA352143615
NM_000335.5:c.4786G>T
CA352143616
NM_000335.5:c.4786G>C