Canonical Allele Identifier: PA2825942561
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201535
ClinVar RCV Id: RCV000183116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Thr1750Ser
CA019145
NM_001160160.2:c.5249C>G
CA352141363
NM_001160160.2:c.5248A>T