Canonical Allele Identifier: PA254769
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9381
ClinVar RCV Id: RCV000009978 RCV000058806 RCV000420298 RCV001841233 RCV002251424 RCV004017231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1923Thr
CA019460
NM_000335.5:c.5767G>A