Canonical Allele Identifier: PA2825588656
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 954171
ClinVar RCV Id: RCV001226581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116538.2:p.Gln604Leu
CA399978449
NM_001123066.4:c.1811A>T