Allele Registry

Canonical Allele Identifier: PA2828704042

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364197.1:p.Ser263Leu	CA225487 NM_001377268.1:c.788C>T