Canonical Allele Identifier: PA307717
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67924
ClinVar RCV Id: RCV000058707 RCV000183085 RCV000247337 RCV000765734 RCV000766805 RCV001150546 RCV001842369 RCV003149713 RCV004528266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1596Ile
CA018565
NM_001099404.2:c.4786T>A