Allele Registry

Canonical Allele Identifier: PA2828703733

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015327

RCV000084549

ClinVar Variation:

14258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364195.1:p.Glu637Val	CA225485 NM_001377266.1:c.1910A>T