Canonical Allele Identifier: PA2825588775
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 323645
ClinVar RCV Id: RCV000356485 RCV000532567 RCV001531268 RCV004526663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116539.1:p.Ala123Thr
CA8617962
NM_001123067.4:c.367G>A