Canonical Allele Identifier: PA346654
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 180517
ClinVar RCV Id: RCV000157491 RCV003539800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro1890Ala
CA019410
NM_000335.5:c.5668C>G