Canonical Allele Identifier: PA2825942708
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68001
ClinVar RCV Id: RCV000058795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Lys1839Asn
CA019389
NM_001160160.2:c.5517G>C
CA352140620
NM_001160160.2:c.5517G>T