Canonical Allele Identifier: PA2827518190
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 212138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337178.1:p.Asp403His
CA207762
NM_001350249.2:c.1207G>C