Canonical Allele Identifier: PA2827923873
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072891
ClinVar RCV Id: RCV004014905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ser1796Thr
CA352141098
NM_001354701.2:c.5386T>A