Canonical Allele Identifier: PA2825942825
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2797141
ClinVar RCV Id: RCV003671042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1912Asp
CA352139771
NM_001160160.2:c.5736G>T
CA352139772
NM_001160160.2:c.5736G>C