Canonical Allele Identifier: PA2825490533
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1907731
ClinVar RCV Id: RCV003591970 RCV003776601 RCV004064546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1601His
CA352143591
NM_001099404.2:c.4802T>A