Canonical Allele Identifier: PA307823
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67974
ClinVar RCV Id: RCV000058760 RCV000183112 RCV001787862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1762Met
CA019062
NM_000335.5:c.5284G>A