Canonical Allele Identifier: PA2827455691
Gene: DENND5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2107907
ClinVar RCV Id: RCV003029335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335678.1:p.Glu136Asp
CA379599772
NM_001348749.2:c.408G>C
CA379599774
NM_001348749.2:c.408G>T