Canonical Allele Identifier: PA2825491777
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519065
ClinVar RCV Id: RCV000619935 RCV001841795 RCV001860378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg8Gln
CA056648
NM_001099405.2:c.23G>A