Canonical Allele Identifier: PA2825493729
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2738493
ClinVar RCV Id: RCV003562643 RCV003591146 RCV004369292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu604Val
CA352146064
NM_001099405.2:c.1810C>G