Canonical Allele Identifier: PA1139760110
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 940929
ClinVar RCV Id: RCV001586051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Leu939Pro
CA352140706
NM_198056.3:c.2816T>C