Allele Registry

Canonical Allele Identifier: PA2826264834

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001190181.1:p.Ser321Leu	CA225487 NM_001203252.2:c.962C>T