Canonical Allele Identifier: PA2826264632
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14252
ClinVar RCV Id: RCV000015321 RCV000084548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190180.1:p.Val277Met
CA225483
NM_001203251.2:c.829G>A