Canonical Allele Identifier: PA2825132106
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072317
ClinVar RCV Id: RCV004012347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1669Val
CA352142778
NM_000335.5:c.5005A>G