Allele Registry

Canonical Allele Identifier: PA915977282

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Gly670Ser	CA225477 NM_001123066.4:c.2008G>A