Canonical Allele Identifier: PA265562
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67881
ClinVar RCV Id: RCV000058661 RCV000246368 RCV003556154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1440Gln
CA018141
NM_000335.5:c.4318G>C