Canonical Allele Identifier: PA2825940210
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3014033
ClinVar RCV Id: RCV003873608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Trp193Arg
CA352153633
NM_001160160.2:c.577T>C
CA352153634
NM_001160160.2:c.577T>A