Canonical Allele Identifier: PA100556
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14252
ClinVar RCV Id: RCV000015321 RCV000084548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Val654Met
CA225483
NM_016835.5:c.1960G>A