Canonical Allele Identifier: PA2825495833
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1332058
ClinVar RCV Id: RCV001842181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asn1325Lys
CA352147630
NM_001099405.2:c.3975T>A
CA352147631
NM_001099405.2:c.3975T>G