Canonical Allele Identifier: PA2825496178
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 389297
ClinVar RCV Id: RCV000424008
ClinVar Variation Id: 2663524
ClinVar RCV Id: RCV003442712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Phe1455Leu
CA16604466
NM_001099405.2:c.4363T>C
CA352145251
NM_001099405.2:c.4365C>G
CA352145252
NM_001099405.2:c.4365C>A