Canonical Allele Identifier: PA2826264653
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14255
ClinVar Variation Id: 98232
ClinVar RCV Id: RCV000084553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Gly329Arg
CA225494
NM_001203251.2:c.985G>C
CA257189
NM_001203251.2:c.985G>A