Canonical Allele Identifier: PA2825495895
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67857
ClinVar RCV Id: RCV000058636 RCV000183060 RCV001146614 RCV001146613 RCV001144668 RCV001144669 RCV001144670 RCV001144671 RCV001535662 RCV001842358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1353Met
CA017837
NM_001099405.2:c.4057G>A