Canonical Allele Identifier: PA265972
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68059
ClinVar RCV Id: RCV000058863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Lys317Asn
CA019950
NM_001099404.2:c.951G>C
CA352150165
NM_001099404.2:c.951G>T