Canonical Allele Identifier: PA329808
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67669
ClinVar RCV Id: RCV000058432 RCV000852550 RCV001842285 RCV003656624 RCV004019035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Phe530Val
CA015032
NM_000335.5:c.1588T>G