Canonical Allele Identifier: PA2580555435
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2452886
ClinVar RCV Id: RCV003177660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala1180Ser
CA352138247
NM_198056.3:c.3538G>T