Canonical Allele Identifier: PA2828704002
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 2978943
ClinVar RCV Id: RCV003839589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Pro175Thr
CA399978212
NM_001377268.1:c.523C>A