Canonical Allele Identifier: PA2825132666
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1901Gln
CA352140265
NM_000335.5:c.5701G>C