Canonical Allele Identifier: PA2825132961
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 345111
ClinVar RCV Id: RCV000287762 RCV000291687 RCV000322026 RCV000346616 RCV000351997 RCV000376753 RCV000403611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp2010Glu
CA10618690
NM_000335.5:c.6030C>A
CA352139019
NM_000335.5:c.6030C>G