Canonical Allele Identifier: PA2826264822
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14268
ClinVar RCV Id: RCV000015338 RCV000084543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Lys286Met
CA225473
NM_001203252.2:c.857A>T