Canonical Allele Identifier: PA2826264614
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 954171
ClinVar RCV Id: RCV001226581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Gln240Leu
CA399978449
NM_001203251.2:c.719A>T