Canonical Allele Identifier: PA2828703741
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364195.1:p.Val658Ile
CA225490
NM_001377266.1:c.1972G>A