Canonical Allele Identifier: PA2825492361
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1044046
ClinVar RCV Id: RCV003770989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg190Pro
CA352153699
NM_001099405.2:c.569G>C