Canonical Allele Identifier: PA143052
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48295
ClinVar RCV Id: RCV000041611 RCV000058525 RCV000157486 RCV000238603 RCV001841599 RCV004018914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val924Ile
CA016475
NM_001099405.2:c.2770G>A