Canonical Allele Identifier: PA100481
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14266
ClinVar RCV Id: RCV000015336 RCV000084517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058519.3:p.Leu583Val
CA225417
NM_016835.5:c.1747C>G