Canonical Allele Identifier: PA2825945362
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67942
ClinVar RCV Id: RCV000058727 RCV000183091 RCV001842373 RCV004019056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Thr1591Met
CA018766
NM_001160161.2:c.4772C>T