Canonical Allele Identifier: PA2825131249
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1396315
ClinVar RCV Id: RCV003657424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1330Val
CA352147578
NM_000335.5:c.3988A>G