Canonical Allele Identifier: PA204246
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67949
ClinVar RCV Id: RCV000058734 RCV000190217 RCV000523560 RCV001842375 RCV002336216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1666Ile
CA018825
NM_000335.5:c.4996G>A