Canonical Allele Identifier: PA2825945307
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072997
ClinVar RCV Id: RCV004015011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Phe1563Leu
CA352143086
NM_001160161.2:c.4689C>G
CA352143087
NM_001160161.2:c.4689C>A
CA352143093
NM_001160161.2:c.4687T>C