Canonical Allele Identifier: PA2825497772
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_001092875.1:p.Asp1993Glu
CA10618690
NM_001099405.2:c.5979C>A
CA352139019
NM_001099405.2:c.5979C>G