Allele Registry

Canonical Allele Identifier: PA2828354148

Gene: DISP1 HGNC NCBI

ClinVar RCV:

RCV000882749

RCV003930580

ClinVar Variation:

711058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356523.1:p.Met1096Thr	CA1409387 NM_001369594.1:c.3287T>C