Canonical Allele Identifier: PA2825132020
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1986789
ClinVar RCV Id: RCV003776966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Lys1640Arg
CA352142962
NM_000335.5:c.4919A>G