Canonical Allele Identifier: PA123829
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_058519.3:p.Asn613del
CA123828
NM_016835.5:c.1838_1840del