Allele Registry

Canonical Allele Identifier: PA225496

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015316

RCV000084554

RCV002476970

ClinVar Variation:

14247

HGVS (amino-acid)	Matching Registered Transcripts
NP_005901.2:p.Arg406Trp	CA225495 NM_005910.6:c.1216C>T