Canonical Allele Identifier: PA2826264554
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 323645
ClinVar RCV Id: RCV000356485 RCV000532567 RCV001531268 RCV004526663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Ala123Thr
CA8617962
NM_001203251.2:c.367G>A