Allele Registry

Canonical Allele Identifier: PA2829854952

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Lys311Ile	CA225492 NM_016834.5:c.932A>T