Allele Registry

Canonical Allele Identifier: PA100546

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015331

RCV000084544

RCV000995804

ClinVar Variation:

14262

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Ser637Phe	CA225475 NM_016835.5:c.1910C>T