Canonical Allele Identifier: PA2825496891
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67965
ClinVar RCV Id: RCV000058751 RCV000762372 RCV000824908 RCV001842380 RCV004019060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1721Trp
CA018994
NM_001099405.2:c.5161C>T