Allele Registry

Canonical Allele Identifier: PA2829628135

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084551

RCV000692998

RCV003905079

ClinVar Variation:

98231

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Val363Ile	CA225490 NM_005910.6:c.1087G>A