Canonical Allele Identifier: PA891860959
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 569420
ClinVar RCV Id: RCV003540674 RCV002283508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val258Ala
CA352150816
NM_198056.3:c.773T>C