Canonical Allele Identifier: PA307598
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201502
ClinVar RCV Id: RCV000183054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Pro1332Ser
CA017710
NM_001099404.2:c.3994C>T