Allele Registry

Canonical Allele Identifier: PA2826264492

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084498

RCV002508758

ClinVar Variation:

14263

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190180.1:p.Arg5Leu	CA225379 NM_001203251.2:c.14G>T