Allele Registry

Canonical Allele Identifier: PA916030553

Gene: DISP1 HGNC NCBI

ClinVar RCV:

RCV000882749

RCV003930580

ClinVar Variation:

711058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337559.1:p.Met853Thr	CA1409387 NM_001350630.2:c.2558T>C