Canonical Allele Identifier: PA100456
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14246
ClinVar RCV Id: RCV000015315 RCV000084519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Gly589Val
CA225421
NM_016835.5:c.1766G>T