Allele Registry

Canonical Allele Identifier: PA915977230

Gene: MAPT HGNC NCBI

ClinVar Allele:

104100

ClinVar RCV:

RCV000084513

RCV000325065

RCV000805364

RCV003935077

RCV003993800

ClinVar Variation:

98208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Ala574Thr	CA225409 NM_001123066.4:c.1720G>A