Allele Registry

Canonical Allele Identifier: PA225478

Gene: MAPT HGNC NCBI

ClinVar Allele:

104120

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Gly652Ser	CA225477 NM_016835.5:c.1954G>A