Canonical Allele Identifier: PA1139759035
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 972689
ClinVar RCV Id: RCV001248781 RCV001253388 RCV001841195 RCV003658785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg693Leu
CA352144827
NM_198056.3:c.2078G>T