Allele Registry

Canonical Allele Identifier: PA2826264825

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Gly304Ser	CA225477 NM_001203252.2:c.910G>A