Allele Registry

Canonical Allele Identifier: PA2828704065

Gene: MAPT HGNC NCBI

ClinVar RCV:

RCV000015316

RCV000084554

RCV002476970

ClinVar Variation:

14247

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364197.1:p.Arg317Trp	CA225495 NM_001377268.1:c.949C>T