Canonical Allele Identifier: PA2825132806
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2736875
ClinVar RCV Id: RCV003560108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro1958Arg
CA352139602
NM_000335.5:c.5873C>G