Canonical Allele Identifier: PA2829628078
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98215
ClinVar RCV Id: RCV000084524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Asn296His
CA225433
NM_005910.6:c.886A>C