Canonical Allele Identifier: PA145124
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1632His
CA018735
NM_198056.3:c.4895G>A