Canonical Allele Identifier: PA658809968
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1980Phe
CA065024
NM_198056.3:c.5938G>T