Canonical Allele Identifier: PA2825489531
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919208
ClinVar RCV Id: RCV001842679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1299Met
CA352148179
NM_001099404.2:c.3897C>G