Canonical Allele Identifier: PA2573074241
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14258
ClinVar RCV Id: RCV000015327 RCV000084549
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364194.1:p.Glu734Val
CA225485
NM_001377265.1:c.2201A>T