Canonical Allele Identifier: PA1139752426
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 925496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly69Asp
CA059672
NM_198056.3:c.206G>A