Canonical Allele Identifier: PA204198
Gene: DIP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207922
ClinVar RCV Id: RCV000190197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996772.1:p.Arg885Gln
CA204197
NM_206889.3:c.2654G>A