Canonical Allele Identifier: PA265648
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67916
ClinVar RCV Id: RCV000058697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1568Pro
CA018491
NM_000335.5:c.4702G>C