Canonical Allele Identifier: PA2825497558
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala1931Ser
CA019500
NM_001099405.2:c.5791G>T