Canonical Allele Identifier: PA2825945436
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 427788
ClinVar RCV Id: RCV000492065 RCV003541189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1647Ile
CA064131
NM_001160161.2:c.4941G>T
CA352142354
NM_001160161.2:c.4941G>C
CA352142355
NM_001160161.2:c.4941G>A