Canonical Allele Identifier: PA218874
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67715
ClinVar RCV Id: RCV000058482 RCV001059141 RCV001842313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser705Phe
CA015866
NM_001099404.2:c.2114C>T