Canonical Allele Identifier: PA2825132351
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 844319
ClinVar RCV Id: RCV001759971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu1771Pro
CA352141533
NM_000335.5:c.5312T>C