Canonical Allele Identifier: PA2825131046
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2725883
ClinVar RCV Id: RCV003554729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr1233Ser
CA352149372
NM_000335.5:c.3698C>G
CA352149391
NM_000335.5:c.3697A>T