Canonical Allele Identifier: PA329822
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg535Gln
CA015071
NM_198056.3:c.1604G>A