Canonical Allele Identifier: PA2826264600
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98208
ClinVar RCV Id: RCV000084513 RCV000325065 RCV000805364 RCV003993800 RCV003935077
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Ala210Thr
CA225409
NM_001203251.2:c.628G>A