Allele Registry

Canonical Allele Identifier: PA915977304

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Ser687Leu	CA225487 NM_001123066.4:c.2060C>T