Canonical Allele Identifier: PA2828703960
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_001364197.1:p.Ala94Thr
CA8617962
NM_001377268.1:c.280G>A