Allele Registry

Canonical Allele Identifier: PA100501

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015338

RCV000084543

ClinVar Variation:

14268

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Lys634Met	CA225473 NM_016835.5:c.1901A>T