Allele Registry

Canonical Allele Identifier: PA915977250

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000084529

RCV002508760

ClinVar Variation:

14269

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Gly638Val	CA225451 NM_001123066.4:c.1913G>T