Canonical Allele Identifier: PA2829854944
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Val305Ile
CA225490
NM_016834.5:c.913G>A