Allele Registry

Canonical Allele Identifier: PA123829

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015334

RCV000015335

RCV000084581

ClinVar Variation:

98243

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Asn613del	CA123828 NM_016835.5:c.1838_1840del