Canonical Allele Identifier: PA2827921268
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 925496
ClinVar RCV Id: RCV003656670 RCV001840998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gly69Asp
CA059672
NM_001354701.2:c.206G>A