Canonical Allele Identifier: PA2825131296
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1737393
ClinVar RCV Id: RCV002321312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1350Ile
CA352147274
NM_000335.5:c.4050G>T
CA352147276
NM_000335.5:c.4050G>C
CA352147278
NM_000335.5:c.4050G>A