Canonical Allele Identifier: PA2825132381
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919539
ClinVar RCV Id: RCV001842702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1783Asp
CA352141338
NM_000335.5:c.5349G>T
CA352141339
NM_000335.5:c.5349G>C