Allele Registry

Canonical Allele Identifier: PA2826264797

Gene: MAPT HGNC NCBI

ClinVar Allele:

104100

ClinVar RCV:

RCV000084513

RCV000325065

RCV000805364

RCV003935077

RCV003993800

ClinVar Variation:

98208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Ala239Thr	CA225409 NM_001203252.2:c.715G>A