Canonical Allele Identifier: PA2827922707
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1213747
ClinVar RCV Id: RCV001591696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Thr1056Ala
CA352139207
NM_001354701.2:c.3166A>G