Canonical Allele Identifier: PA2827923044
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67827
ClinVar RCV Id: RCV000058603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Trp1270Cys
CA017524
NM_001354701.2:c.3810G>C
CA352148951
NM_001354701.2:c.3810G>T