Canonical Allele Identifier: PA2827923713
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1057952
ClinVar RCV Id: RCV001367028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ser1699Arg
CA064180
NM_001354701.2:c.5097C>A
CA352142161
NM_001354701.2:c.5097C>G
CA352142170
NM_001354701.2:c.5095A>C