Canonical Allele Identifier: PA2825131051
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1305091
ClinVar RCV Id: RCV001773801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr1240Cys
CA352149290
NM_000335.5:c.3719A>G