Canonical Allele Identifier: PA2826264814
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14246
ClinVar RCV Id: RCV000015315 RCV000084519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Gly272Val
CA225421
NM_001203252.2:c.815G>T