Canonical Allele Identifier: PA2827922700
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463321
ClinVar RCV Id: RCV000541406 RCV001578235 RCV003999078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala1052Asp
CA352139258
NM_001354701.2:c.3155C>A