Canonical Allele Identifier: PA2827922078
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 834942
ClinVar RCV Id: RCV003541099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu625Asp
CA058996
NM_001354701.2:c.1875G>C
CA352145820
NM_001354701.2:c.1875G>T