Allele Registry

Canonical Allele Identifier: PA1139676620

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015334

RCV000015335

RCV000084581

ClinVar Variation:

98243

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Asn631del	CA123828 NM_001123066.4:c.1892_1894del