Canonical Allele Identifier: PA2825945957
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Pro1952Ala
CA019597
NM_001160161.2:c.5854C>G