Canonical Allele Identifier: PA645506394
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 207974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1898His
CA064651
NM_198056.3:c.5693G>A