Canonical Allele Identifier: PA2825132735
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Phe1927Val
CA352139966
NM_000335.5:c.5779T>G