Canonical Allele Identifier: PA645505685
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 418616
ClinVar RCV Id: RCV000481094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Tyr1447His
CA16617946
NM_198056.3:c.4339T>C