Canonical Allele Identifier: PA2826264568
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98205
ClinVar RCV Id: RCV000084510 RCV000246861 RCV000387650 RCV001079276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Ala149Thr
CA225403
NM_001203251.2:c.445G>A