Canonical Allele Identifier: PA2827923744
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_001341630.1:p.Gly1721Arg
CA019005
NM_001354701.2:c.5161G>A
CA352141917
NM_001354701.2:c.5161G>C