Canonical Allele Identifier: PA2825493775
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 928169
ClinVar RCV Id: RCV002484054 RCV001841157 RCV003541290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg620His
CA058963
NM_001099405.2:c.1859G>A