Canonical Allele Identifier: PA2826264496
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 1335279
ClinVar RCV Id: RCV001815827 RCV001869641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Glu9Lys
CA8617496
NM_001203251.2:c.25G>A