Allele Registry

Canonical Allele Identifier: PA100536

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015323

RCV000084530

ClinVar Variation:

14254

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Ser622Asn	CA225453 NM_016835.5:c.1865G>A