Canonical Allele Identifier: PA2825588891
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14255
ClinVar RCV Id: RCV000517183 RCV001851871 RCV000015324
ClinVar Variation Id: 98232
ClinVar RCV Id: RCV000084553
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Gly360Arg
CA225494
NM_001123067.4:c.1078G>C
CA257189
NM_001123067.4:c.1078G>A