Canonical Allele Identifier: PA2825493834
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2876538
ClinVar RCV Id: RCV003710341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Thr630Arg
CA352145765
NM_001099405.2:c.1889C>G