Allele Registry

Canonical Allele Identifier: PA2826649333

Gene: ADNP HGNC NCBI

ClinVar RCV:

RCV000499393

RCV000764249

RCV001545023

ClinVar Variation:

434095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269460.1:p.Asp873Tyr	CA9908560 NM_001282531.3:c.2617G>T