Canonical Allele Identifier: PA2825939959
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463363
ClinVar RCV Id: RCV000532753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gln32Arg
CA352158965
NM_001160160.2:c.95A>G