Allele Registry

Canonical Allele Identifier: PA100471

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015324

RCV000084553

RCV000517183

RCV001851871

ClinVar Variation:

14255

98232

HGVS (amino-acid)	Matching Registered Transcripts
NP_058519.3:p.Gly706Arg	CA225494 NM_016835.5:c.2116G>C CA257189 NM_016835.5:c.2116G>A