Allele Registry

Canonical Allele Identifier: PA2825588712

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084498

RCV002508758

ClinVar Variation:

14263

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Arg5Leu	CA225379 NM_001123067.4:c.14G>T