Allele Registry

Canonical Allele Identifier: PA2829854845

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015336

RCV000084517

ClinVar Variation:

14266

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Leu208Val	CA225417 NM_016834.5:c.622C>G