Canonical Allele Identifier: PA2825494726
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201482
ClinVar RCV Id: RCV000183014 RCV002433808 RCV003591707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp953Glu
CA016578
NM_001099405.2:c.2859C>G
CA352140500
NM_001099405.2:c.2859C>A