Canonical Allele Identifier: PA2827921493
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68038
ClinVar RCV Id: RCV000058841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ile239Val
CA019755
NM_001354701.2:c.715A>G