Canonical Allele Identifier: PA2825588863
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14268
ClinVar RCV Id: RCV000015338 RCV000084543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Lys288Met
CA225473
NM_001123067.4:c.863A>T