Canonical Allele Identifier: PA2827923159
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406429
ClinVar RCV Id: RCV003317213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu1341Phe
CA16611264
NM_001354701.2:c.4021C>T