Allele Registry

Canonical Allele Identifier: PA2829628012

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084513

RCV000325065

RCV000805364

RCV003935077

RCV003993800

ClinVar Variation:

98208

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Ala239Thr	CA225409 NM_005910.6:c.715G>A