Canonical Allele Identifier: PA225418
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Leu266Val
CA225417
NM_005910.6:c.796C>G