Canonical Allele Identifier: PA2825495561
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67817
ClinVar RCV Id: RCV000058592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu1239Pro
CA017455
NM_001099405.2:c.3716T>C