Allele Registry

Canonical Allele Identifier: PA2829628095

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV001663503

RCV001825013

ClinVar Variation:

1256161

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Ser305Ile	CA399983393 NM_005910.6:c.914G>T