Canonical Allele Identifier: PA329833
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala572Val
CA015275
NM_001099404.2:c.1715C>T