Canonical Allele Identifier: PA2825588897
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Arg377Trp
CA225495
NM_001123067.4:c.1129C>T