Canonical Allele Identifier: PA2829855604
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98205
ClinVar RCV Id: RCV000084510 RCV000246861 RCV000387650 RCV001079276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058525.1:p.Ala120Thr
CA225403
NM_016841.5:c.358G>A