Canonical Allele Identifier: PA2828704047
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Val274Ile
CA225490
NM_001377268.1:c.820G>A