Canonical Allele Identifier: PA330278
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala1949Ser
CA019500
NM_001099404.2:c.5845G>T