Canonical Allele Identifier: PA2829855725
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_058525.1:p.Glu253Val
CA225485
NM_016841.5:c.758A>T