Allele Registry

Canonical Allele Identifier: PA2499255661

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015334

RCV000015335

RCV000084581

ClinVar Variation:

98243

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Asn688del	CA123828 NM_001377265.1:c.2063_2065del