Canonical Allele Identifier: PA2825129488
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 927347
ClinVar RCV Id: RCV001841109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln575Glu
CA352146502
NM_000335.5:c.1723C>G