Canonical Allele Identifier: PA2825942782
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 922050
ClinVar RCV Id: RCV001843110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ser1887Ala
CA352140059
NM_001160160.2:c.5659T>G