Canonical Allele Identifier: PA181481
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67920
ClinVar RCV Id: RCV000058701 RCV000154836 RCV001289206 RCV001842368 RCV004019052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1582Cys
CA018516
NM_000335.5:c.4744C>T