Allele Registry

Canonical Allele Identifier: PA2829854925

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015338

RCV000084543

ClinVar Variation:

14268

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Lys259Met	CA225473 NM_016834.5:c.776A>T