Canonical Allele Identifier: PA2825942795
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe1895Val
CA352139966
NM_001160160.2:c.5683T>G