Canonical Allele Identifier: PA265820
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67971
ClinVar RCV Id: RCV000058757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Lys175Asn
CA019045
NM_001099404.2:c.525G>C
CA352153868
NM_001099404.2:c.525G>T