Canonical Allele Identifier: PA2825132864
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 963939
ClinVar RCV Id: RCV003656727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1975Ala
CA352139436
NM_000335.5:c.5923T>G