Canonical Allele Identifier: PA2825494035
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67708
ClinVar RCV Id: RCV000058475 RCV001842307 RCV003764735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Cys683Gly
CA015785
NM_001099405.2:c.2047T>G