Canonical Allele Identifier: PA2827923100
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 917997
ClinVar RCV Id: RCV001175242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1305Ser
CA352148145
NM_001354701.2:c.3913C>A