Allele Registry

Canonical Allele Identifier: PA2829854932

Gene: MAPT HGNC NCBI

ClinVar Allele:

104120

ClinVar RCV:

RCV000084545

RCV003514309

ClinVar Variation:

98228

HGVS (amino-acid)	Matching Registered Transcripts
NP_058518.1:p.Gly277Ser	CA225477 NM_016834.5:c.829G>A