Canonical Allele Identifier: PA2825942757
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1428511
ClinVar RCV Id: RCV003772861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1872Gly
CA352140224
NM_001160160.2:c.5615C>G