Canonical Allele Identifier: PA2828703753
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_001364195.1:p.Gly684Arg
CA225494
NM_001377266.1:c.2050G>C
CA257189
NM_001377266.1:c.2050G>A