Canonical Allele Identifier: PA2825945850
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406424
ClinVar RCV Id: RCV003766539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Tyr1896Gln
CA16611272
NM_001160161.2:c.5686_5688delinsCAA