Allele Registry

Canonical Allele Identifier: PA2825588848

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015334

RCV000015335

RCV000084581

ClinVar Variation:

98243

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Asn267del	CA123828 NM_001123067.4:c.800_802del