Canonical Allele Identifier: PA2825940229
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68028
ClinVar RCV Id: RCV000058828 RCV003989314 RCV003996554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala204Val
CA019639
NM_001160160.2:c.611C>T