Allele Registry

Canonical Allele Identifier: PA915977241

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015315

RCV000084519

ClinVar Variation:

14246

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116538.2:p.Gly607Val	CA225421 NM_001123066.4:c.1820G>T