Canonical Allele Identifier: PA2829628079
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98243
ClinVar RCV Id: RCV000015335 RCV000015334 RCV000084581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005901.2:p.Asn296del
CA123828
NM_005910.6:c.887_889del