Allele Registry

Canonical Allele Identifier: PA2829628113

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Gly335Ser	CA225477 NM_005910.6:c.1003G>A