Allele Registry

Canonical Allele Identifier: PA2826264629

Gene: MAPT HGNC NCBI

ClinVar Allele:

104120

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Gly275Ser	CA225477 NM_001203251.2:c.823G>A