Allele Registry

Canonical Allele Identifier: PA2826264850

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015324

RCV000084553

RCV000517183

RCV001851871

ClinVar Variation:

14255

98232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Gly358Arg	CA225494 NM_001203252.2:c.1072G>C CA257189 NM_001203252.2:c.1072G>A