Canonical Allele Identifier: PA2825130207
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2855874
ClinVar RCV Id: RCV003701629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu908Val
CA352141516
NM_000335.5:c.2723A>T