Canonical Allele Identifier: PA2825491964
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 987810
ClinVar RCV Id: RCV001269146 RCV001701311 RCV001880173 RCV002402807 RCV004004938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg53Trp
CA72951821
NM_001099405.2:c.157C>T