Canonical Allele Identifier: PA916005950
Gene: DDC HGNC NCBI

Linked Data

ClinVar Variation Id: 17812
ClinVar RCV Id: RCV000019390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229817.2:p.Ser69Arg
CA127448
NM_001242888.2:c.205A>C
CA367526855
NM_001242888.2:c.207T>G
CA367526856
NM_001242888.2:c.207T>A