Canonical Allele Identifier: PA2829628004
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 2978943
ClinVar RCV Id: RCV003839589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Pro233Thr
CA399978212
NM_005910.6:c.697C>A