Canonical Allele Identifier: PA107439
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68015
ClinVar RCV Id: RCV000058812 RCV000148844 RCV000212995 RCV000987194 RCV001842397 RCV002354251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1958Gln
CA019519
NM_198056.3:c.5873G>A