Allele Registry

Canonical Allele Identifier: PA2829855705

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015331

RCV000084544

RCV000995804

ClinVar Variation:

14262

HGVS (amino-acid)	Matching Registered Transcripts
NP_058525.1:p.Ser231Phe	CA225475 NM_016841.5:c.692C>T