Allele Registry

Canonical Allele Identifier: PA100411

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084498

RCV002508758

ClinVar Variation:

14263

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Arg5Leu	CA225379 NM_016835.5:c.14G>T