Canonical Allele Identifier: PA330075
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1486Leu
CA018283
NM_000335.5:c.4456A>C
CA352144358
NM_000335.5:c.4456A>T