Canonical Allele Identifier: PA2825945846
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala1895Ser
CA019500
NM_001160161.2:c.5683G>T