Canonical Allele Identifier: PA2825491411
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3073178
ClinVar RCV Id: RCV004015192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr1893Ala
CA352140356
NM_001099404.2:c.5677A>G