Canonical Allele Identifier: PA108395
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67845
ClinVar RCV Id: RCV000058624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser1333Tyr
CA017732
NM_198056.3:c.3998C>A