Canonical Allele Identifier: PA2825132790
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2501845
ClinVar RCV Id: RCV003228264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1950Ala
CA352139701
NM_000335.5:c.5849T>C