Canonical Allele Identifier: PA2825132933
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3027196
ClinVar RCV Id: RCV003887589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro2005del
CA542269470
NM_000335.5:c.6012_6014del