Canonical Allele Identifier: PA2825942313
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67937
ClinVar RCV Id: RCV000058721 RCV000489058 RCV000709763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1596Gln
CA018714
NM_001160160.2:c.4787G>A