Canonical Allele Identifier: PA2825496253
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu1483Val
CA018357
NM_001099405.2:c.4447C>G