Allele Registry

Canonical Allele Identifier: PA2828703753

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015324

RCV000084553

RCV000517183

RCV001851871

ClinVar Variation:

14255

98232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364195.1:p.Gly684Arg	CA225494 NM_001377266.1:c.2050G>C CA257189 NM_001377266.1:c.2050G>A