Canonical Allele Identifier: PA107466
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68043
ClinVar RCV Id: RCV000058846 RCV000234990 RCV000713149 RCV000987245 RCV001842412 RCV002415517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg27His
CA019812
NM_198056.3:c.80G>A