Canonical Allele Identifier: PA2825132751
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 582721
ClinVar RCV Id: RCV000764501 RCV001841875 RCV000852962 RCV002352218 RCV003540842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1931Val
CA064808
NM_000335.5:c.5792C>T