Canonical Allele Identifier: PA2825489687
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3008823
ClinVar RCV Id: RCV003861950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1335Val
CA72944913
NM_001099404.2:c.4003A>G