Canonical Allele Identifier: PA107398
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1644His
CA018760
NM_198056.3:c.4931G>A