Canonical Allele Identifier: PA2825491984
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3009723
ClinVar RCV Id: RCV003864834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Lys62Arg
CA352158301
NM_001099405.2:c.185A>G