Allele Registry

Canonical Allele Identifier: PA2829854936

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Glu284Val	CA225485 NM_016834.5:c.851A>T