Canonical Allele Identifier: PA2825942940
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Pro1973Ala
CA019597
NM_001160160.2:c.5917C>G