Canonical Allele Identifier: PA2829854927
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058518.1:p.Ser262Phe
CA225475
NM_016834.5:c.785C>T