Canonical Allele Identifier: PA265804
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67966
ClinVar RCV Id: RCV000058752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1739Arg
CA019005
NM_000335.5:c.5215G>A
CA352141917
NM_000335.5:c.5215G>C