Canonical Allele Identifier: PA2825495552
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67816
ClinVar RCV Id: RCV000058591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Lys1236Asn
CA017441
NM_001099405.2:c.3708G>T
CA352149346
NM_001099405.2:c.3708G>C