Allele Registry

Canonical Allele Identifier: PA2829628079

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015334

RCV000015335

RCV000084581

ClinVar Variation:

98243

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Asn296del	CA123828 NM_005910.6:c.887_889del