Canonical Allele Identifier: PA218885
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67767
ClinVar RCV Id: RCV000058537 RCV001842321 RCV002477198 RCV004019044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg975Trp
CA016625
NM_001099404.2:c.2923C>T