Canonical Allele Identifier: PA2827923163
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe1343Leu
CA017772
NM_001354701.2:c.4027T>C
CA352147403
NM_001354701.2:c.4029C>G
CA352147404
NM_001354701.2:c.4029C>A