Canonical Allele Identifier: PA143123
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1903Leu
CA019439
NM_000335.5:c.5708C>T