Allele Registry

Canonical Allele Identifier: PA257192

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015330

RCV000266864

ClinVar Variation:

14261

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Arg5His	CA257191 NM_005910.6:c.14G>A