Canonical Allele Identifier: PA2827924058
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe1909Val
CA352139966
NM_001354701.2:c.5725T>G