Canonical Allele Identifier: PA181524
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala286Ser
CA019856
NM_001099404.2:c.856G>T