Allele Registry

Canonical Allele Identifier: PA2825588866

Gene: MAPT HGNC NCBI

ClinVar Allele:

104120

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116539.1:p.Gly306Ser	CA225477 NM_001123067.4:c.916G>A