Canonical Allele Identifier: PA2825491853
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000041
ClinVar RCV Id: RCV001296119 RCV003591852 RCV003541320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met28Ile
CA352159056
NM_001099405.2:c.84G>T
CA352159058
NM_001099405.2:c.84G>C
CA352159062
NM_001099405.2:c.84G>A