Canonical Allele Identifier: PA2828704032
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364197.1:p.Ser231Phe
CA225475
NM_001377268.1:c.692C>T