Canonical Allele Identifier: PA2827502629
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 212138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337175.1:p.Asp200His
CA207762
NM_001350246.2:c.598G>C