Canonical Allele Identifier: PA2825940821
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2146111
ClinVar RCV Id: RCV003658756 RCV004009339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.His617Arg
CA352145914
NM_001160160.2:c.1850A>G