Allele Registry

Canonical Allele Identifier: PA2573074249

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015324

RCV000084553

RCV000517183

RCV001851871

ClinVar Variation:

14255

98232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364194.1:p.Gly781Arg	CA225494 NM_001377265.1:c.2341G>C CA257189 NM_001377265.1:c.2341G>A