Canonical Allele Identifier: PA2825939916
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 928310
ClinVar RCV Id: RCV001760149 RCV001841168 RCV001245113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro7Ser
CA72951858
NM_001160160.2:c.19C>T