Canonical Allele Identifier: PA2825942730
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463350
ClinVar RCV Id: RCV003238767 RCV003591748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Tyr1856Cys
CA72937852
NM_001160160.2:c.5567A>G