Canonical Allele Identifier: PA2825495036
Gene: SCN5A HGNC NCBI
ClinVar RCV:
RCV001591696
ClinVar Variation:
1213747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Thr1056Ala
CA352139207
NM_001099405.2:c.3166A>G