Canonical Allele Identifier: PA2825130290
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774465
ClinVar RCV Id: RCV003592348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp953Gly
CA352140504
NM_000335.5:c.2858A>G