Allele Registry

Canonical Allele Identifier: PA2828704053

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015329

RCV000084552

ClinVar Variation:

14260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364197.1:p.Lys280Ile	CA225492 NM_001377268.1:c.839A>T