Canonical Allele Identifier: PA2825497148
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_001092875.1:p.Ser1797Thr
CA352141098
NM_001099405.2:c.5389T>A