Canonical Allele Identifier: PA225491
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Val680Ile
CA225490
NM_016835.5:c.2038G>A