Canonical Allele Identifier: PA2825939982
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67654
ClinVar RCV Id: RCV000058412 RCV003298118 RCV001842274 RCV003319178 RCV003654189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg43Gln
CA014665
NM_001160160.2:c.128G>A