Canonical Allele Identifier: PA915970687
Gene: PSMD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 726032
ClinVar RCV Id: RCV000900188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002805.1:p.Gly226Asp
CA10486662
NM_002814.4:c.677G>A