Canonical Allele Identifier: PA265610
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904
ClinVar RCV Id: RCV000058684 RCV000756618 RCV000709759 RCV001201272 RCV001842366 RCV003162459 RCV004537262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1501Val
CA018357
NM_001099404.2:c.4501C>G