Allele Registry

Canonical Allele Identifier: PA225488

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Ser352Leu	CA225487 NM_005910.6:c.1055C>T