Allele Registry

Canonical Allele Identifier: PA2829855729

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_058525.1:p.Ser263Leu	CA225487 NM_016841.5:c.788C>T