Canonical Allele Identifier: PA2829855705
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058525.1:p.Ser231Phe
CA225475
NM_016841.5:c.692C>T