Canonical Allele Identifier: PA2825941859
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519131
ClinVar RCV Id: RCV000618029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1305Leu
CA352148142
NM_001160160.2:c.3914G>T