Canonical Allele Identifier: PA658809933
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ile1853Val
CA352140852
NM_198056.3:c.5557A>G