Canonical Allele Identifier: PA2826264716
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 98196
ClinVar RCV Id: RCV000084501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190181.1:p.Gly86Ser
CA225385
NM_001203252.2:c.256G>A