Canonical Allele Identifier: PA2829855377
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 966198
ClinVar RCV Id: RCV001240818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Pro587Leu
CA291107190
NM_016835.5:c.1760C>T