Canonical Allele Identifier: PA307095
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201428
ClinVar Variation Id: 242209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala29Val
CA019870
NM_000335.5:c.86_87delinsTG
CA019875
NM_000335.5:c.86C>T