Canonical Allele Identifier: PA2830432956
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074125
ClinVar RCV Id: RCV004012667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp1792Glu
CA72937945
NM_198056.3:c.5376T>A
CA352141253
NM_198056.3:c.5376T>G