Canonical Allele Identifier: PA2827923886
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 936302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Pro1805Leu
CA352141039
NM_001354701.2:c.5414C>T