Canonical Allele Identifier: PA2825491270
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2633114
ClinVar RCV Id: RCV004531619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1846Glu
CA352140895
NM_001099404.2:c.5538C>G
CA352140896
NM_001099404.2:c.5538C>A