Canonical Allele Identifier: PA2825129454
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 925641
ClinVar RCV Id: RCV001841009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro564Ser
CA352146692
NM_000335.5:c.1690C>T