Canonical Allele Identifier: PA645506443
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406424
ClinVar RCV Id: RCV003766539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Tyr1950Gln
CA16611272
NM_198056.3:c.5848_5850delinsCAA