Allele Registry

Canonical Allele Identifier: PA2829854939

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084550

RCV002508759

ClinVar Variation:

14267

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Ser294Leu	CA225487 NM_016834.5:c.881C>T