Canonical Allele Identifier: PA2826264633
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14258
ClinVar RCV Id: RCV000015327 RCV000084549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Glu282Val
CA225485
NM_001203251.2:c.845A>T