Canonical Allele Identifier: PA211815
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67985
ClinVar RCV Id: RCV000058771 RCV000148849 RCV000183115 RCV000617171 RCV001146113 RCV001146114 RCV001146115 RCV001146116 RCV001146117 RCV000786219 RCV001146112 RCV001842384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr1778Met
CA019134
NM_000335.5:c.5333C>T