Canonical Allele Identifier: PA2825497315
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923198
ClinVar RCV Id: RCV001843179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1842Ser
CA352140762
NM_001099405.2:c.5526G>T
CA352140763
NM_001099405.2:c.5526G>C