Canonical Allele Identifier: PA2825131086
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1356845
ClinVar RCV Id: RCV003657351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1261Cys
CA352149068
NM_000335.5:c.3781G>T