Canonical Allele Identifier: PA2828703709
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98210
ClinVar RCV Id: RCV000084516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364195.1:p.Ile586Val
CA225415
NM_001377266.1:c.1756A>G