Canonical Allele Identifier: PA225441
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14256
ClinVar RCV Id: RCV000015325 RCV000084526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Pro272Ser
CA225439
NM_001123067.4:c.814C>T