Allele Registry

Canonical Allele Identifier: PA2573074237

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Gly727Ser	CA225477 NM_001377265.1:c.2179G>A