Canonical Allele Identifier: PA265671
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67921
ClinVar RCV Id: RCV000058702 RCV000413021 RCV000455572 RCV003996544 RCV004019053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1582His
CA018522
NM_000335.5:c.4745G>A