Allele Registry

Canonical Allele Identifier: PA2826264838

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084551

RCV000692998

RCV003905079

ClinVar Variation:

98231

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Val332Ile	CA225490 NM_001203252.2:c.994G>A