Canonical Allele Identifier: PA2827921259
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435759
ClinVar RCV Id: RCV003136509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala60Thr
CA352158333
NM_001354701.2:c.178G>A