Canonical Allele Identifier: PA916030369
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 212138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337177.1:p.Asp533His
CA207762
NM_001350248.2:c.1597G>C