Canonical Allele Identifier: PA2825129609
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2989089
ClinVar RCV Id: RCV003849240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp629Gly
CA352145780
NM_000335.5:c.1886A>G