Allele Registry

Canonical Allele Identifier: PA2825588875

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Ser323Leu	CA225487 NM_001123067.4:c.968C>T