Canonical Allele Identifier: PA2826264617
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_001190180.1:p.Gly243Val
CA225421
NM_001203251.2:c.728G>T