Allele Registry

Canonical Allele Identifier: PA225443

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015325

RCV000084526

ClinVar Variation:

14256

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Pro636Ser	CA225439 NM_001123066.4:c.1906C>T