Allele Registry

Canonical Allele Identifier: PA2826264636

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Ser292Leu	CA225487 NM_001203251.2:c.875C>T