Allele Registry

Canonical Allele Identifier: PA2829855736

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084551

RCV000692998

RCV003905079

ClinVar Variation:

98231

HGVS (amino-acid)	Matching Registered Transcripts
NP_058525.1:p.Val274Ile	CA225490 NM_016841.5:c.820G>A