Canonical Allele Identifier: PA143124
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1904Leu
CA019439
NM_001099404.2:c.5711C>T