Canonical Allele Identifier: PA2825941471
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 639665
ClinVar RCV Id: RCV003540869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1061Asp
CA061337
NM_001160160.2:c.3183A>C
CA352139126
NM_001160160.2:c.3183A>T